Original source

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

C/- | Ancestral: C | MAF: < 0.01 (-)

Chromosome 9:97678875 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs368692213, rs138496582

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays