Original source

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

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

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

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

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