Original source

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

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

Chromosome 3:49694428 (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.49694428G>T
ENST00000454491.2:c.168-2715G>T
ENST00000327697.7:c.168-2715G>T
ENST00000432042.2:c.-191-2935G>T
ENST00000487805.3:n.246-2715G>T
ENST00000443204.1:c.168-2617G>T
ENST00000457726.2:c.168-2715G>T
ENST00000486102.2:n.249-2715G>T

This variation has assays on 5 chips - click the plus to show

Variation displays