Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.13 (G)
Location

Chromosome 7:31015565 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59653211, rs52835078

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

This variation has assays on 7 chips - click the plus to show

Variation displays