Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.01 (A)

Chromosome 5:159316780 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2817 sample genotypes and is mentioned in 6 citations.

Variant displays