Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ambiguity code: W
Location

Chromosome 12:32858127 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57149524

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1 individual genotype.

Variation displays