Original source

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

Alleles
T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.07 (A)
Location

Chromosome 17:61996199 (forward strand) | View in location tab

Co-located

with dbSNP rs41318507 (A/G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17841596

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

Variation displays