Original source

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

Alleles
T/C/G | Ambiguity code: B
Location

Chromosome 5:162106919 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117115163

This variation has 14 HGVS names - click the plus to show

Variation displays