Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.34 (-)
Location

Chromosome 2:174751339 (forward strand) | View in location tab

Co-located

with dbSNP rs149000086 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144230187, rs371511301

This variation has 7 HGVS names - click the plus to show

Variation displays