Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 5:150122118 (forward strand) | View in location tab

Co-located

with dbSNP rs67620629 (T/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs62621923

This variation has 5 HGVS names - click the plus to show

Variation displays