Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.22 (T)
Location

Chromosome 3:49731861 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs13071817

This variation has 8 HGVS names - click the plus to show

3:g.49731861G>T
ENST00000454491.1:c.168-2715G>T
ENST00000327697.6:c.168-2715G>T
ENST00000432042.1:c.-191-2935G>T
ENST00000487805.2:n.246-2715G>T
ENST00000443204.1:c.168-2617G>T
ENST00000457726.1:c.168-2715G>T
ENST00000486102.1:n.249-2715G>T

This variation has assays on 4 chips - click the plus to show

Variation displays