Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 1:161206230 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17397986

This variation has 32 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays