Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.08 (A)
Location

Chromosome 9:27570156 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58703505

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 1385 individual genotypes.

Variation displays