Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 9:72772431 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 33506428

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays