Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.46 (A)
Location

Chromosome 17:41274906 (forward strand) | View in location tab

Co-located

with dbSNP rs199839105 (G/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1180358, rs8176084

This variation has 28 HGVS names - click the plus to show

Variation displays