Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.45 (A)

Chromosome 4:73419850 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17795977

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2586 sample genotypes.

Variant displays