Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (C)
Location

Chromosome 14:74902643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3199989, rs61044770

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2627 individual genotypes.

Variation displays