Genetics Genetics Research
CHROMOSOME X HTR2C Xq23 GENE VIEW HTR2C · Xq23 Xq22 Xq24 rs1414334 — ~70,000 base pairs in the gene — ~14,000 uncommon variants · <1% of humans have them — ~1,000 common variants · >1% carry the alternate allele ALLELE STATE rs1414334 C / A · HTR2C · Xq23 HOMOZYGOUS WILD TYPE (DOMINANT) 5′ 3′ C 5′ 3′ C HETEROZYGOUS 5′ 3′ C 5′ 3′ A HOMOZYGOUS ALTERNATE (RECESSIVE) 5′ 3′ A 5′ 3′ A C Cytosine — reference allele A Adenine — variant allele genetics.jdge.cc

rs1414334

Gene: HTR2C — 5-Hydroxytryptamine Receptor 2C Chr X:114903581 Xq23 Intron Variant
NCBI ↗ GeneCards ↗ Open Targets ↗ gnomAD ↗ OMIM ↗ ClinVar ↗ Varsome ↗ LOVD ↗

Population Frequencies9

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Total C 0.21489G 0.78511CC 0.138978CG/GC 0.15182GG 0.709202pop=24,450 ↬
African C 0.455G 0.545CC 0.296915CG/GC 0.316152GG 0.386933pop=5,510
African American C 0.4555G 0.5445CC 0.297246CG/GC 0.316484GG 0.386269pop=5,302
African Others C 0.442G 0.558CC 0.288462CG/GC 0.307692GG 0.403846pop=208
European C 0.14476G 0.85524CC 0.094464CG/GC 0.100589GG 0.804947pop=16,980
Latin American 1 C 0.167G 0.833CC 0.061404CG/GC 0.210526GG 0.72807pop=228
Latin American 2 C 0.087G 0.913CC 0.042394CG/GC 0.089776GG 0.86783pop=802
Other C 0.235G 0.765CC 0.145658CG/GC 0.179272GG 0.67507pop=714
South Asian C 0.127G 0.873CC 0.058824CG/GC 0.137255GG 0.803922pop=102

Studies0

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No new studies.

Curated Studies0 ▼

These studies were determined to be useful for this variant — check "Unused Studies" further down if curious what didn't make the cut.

No curated studies yet.

Unused Studies0 ▼

No unused studies.