Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 14:102135598 (forward strand) | View in location tab

Co-located

with dbSNP rs79180147 (A/G), rs111882928 (C/T), rs113903190 (A/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs10311481, rs1771020

This variation has 4 HGVS names - click the plus to show

Variation displays