Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.27 (T)

Chromosome 18:902964 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs61563249

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2767 sample genotypes.

Variant displays