Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.31 (T)
Location

Chromosome 15:73929861 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56431870, rs57313558

This variation has 3 HGVS names - click the plus to show

15:g.73929861T>C
ENST00000566011.2:c.1102+1976T>C
ENST00000261921.7:c.1102+1976T>C

This variation has assays on 10 chips - click the plus to show

Variation displays