Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.10 (T)
Location

Chromosome 1:110111239 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17516999, rs60716285

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

Variation displays