Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.20 (T)
Location

Chromosome 3:49694428 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs13071817

This variant has 9 HGVS names - click the plus to show

3:g.49694428G>T
ENST00000454491.5:c.168-2715G>T
ENST00000327697.10:c.168-2715G>T
ENST00000432042.5:c.-191-2935G>T
ENST00000487805.6:n.246-2715G>T
ENST00000443204.3:c.168-2617G>T
ENST00000629802.1:c.168-2617G>T
ENST00000457726.5:c.168-2715G>T
ENST00000486102.5:n.249-2715G>T

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

About this variant

This variant overlaps 10 transcripts, has 2624 sample genotypes and is mentioned in 1 citation.

Variant displays