Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.07 (C)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs67930310

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2506 sample genotypes.

Variant displays