Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.09 (C)

Chromosome 15:66384994 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs67930310

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

About this variant

This variant overlaps 7 transcripts and has 1101 individual genotypes.

Variation displays