Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.22 (G)

Chromosome 11:68340003 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs170256, rs664003

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1097 individual genotypes.

Variation displays