Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.48 (A)
Location

Chromosome 11:102463607 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7949109

This variation has 2 HGVS names - click the plus to show

Variation displays