Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (C)

Chromosome 1:167281115 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2844 sample genotypes.

Variant displays