Original source

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

T/C/G | Ancestral: G | Ambiguity code: B | MAF: 0.25 (T)

Chromosome 6:161515785 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs118125375, rs60603650

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 1274 individual genotypes.

Variation displays