Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.35 (A)
Location

Chromosome 6:161174138 (forward strand) | View in location tab

Co-located

with dbSNP rs57037765 (A/G)

Most severe consequence
Evidence status

Synonyms

This variation has 3 HGVS names - click the plus to show

Variation displays