Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.06 (A)
Location

Chromosome 9:95191097 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs374952

This variation has 8 HGVS names - click the plus to show

Variation displays