Original source

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

-/A | MAF: 0.12 (A)

Chromosome 7: between 151573142 and 151573143 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs146040967, rs374204532

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2504 sample genotypes.

Variant displays