Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/- | Ancestral: T | MAF: 0.26 (-)

Chromosome 16:74736059 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs141975099, rs373932135

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2509 sample genotypes.

Variant displays