Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 16:31368874 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58681810, rs56622927

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

16:g.31368874T>C
ENST00000562522.1:c.430+189T>C
ENST00000268296.4:c.430+189T>C
ENST00000562918.1:n.619T>C
ENST00000567409.1:n.837T>C

This variation has assays on 12 chips - click the plus to show

Variation displays