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 9 HGVS names - click the plus to show

3:g.49694428G>T
ENST00000454491.4:c.168-2715G>T
ENST00000327697.9:c.168-2715G>T
ENST00000432042.4:c.-191-2935G>T
ENST00000487805.5:n.246-2715G>T
ENST00000443204.2:c.168-2617G>T
ENST00000629802.1:c.168-2617G>T
ENST00000457726.4:c.168-2715G>T
ENST00000486102.4:n.249-2715G>T

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

About this variant

This variant overlaps 10 transcripts, has 2114 individual genotypes and is mentioned in 1 citation.

Variation displays