Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 14:101963507 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17511820

HGVS name

14:g.101963507T>C

About this variant

This variant overlaps 1 transcript and has 1179 individual genotypes.

Variation displays