Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.20 (G)
Location

Chromosome 3:171027131 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR052438

Most severe consequence
Evidence status

HGVS name

3:g.171027131T>G

This variation has assays on 4 chips - click the plus to show

Variation displays