Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 5:161873225 (forward strand) | View in location tab

Most severe consequence

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 26 individual genotypes.

Variation displays