Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.06 (A)

Chromosome 1:169467915 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs116971455, rs60335656

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2775 sample genotypes.

Variant displays