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: 0.30 (T)
Location

Chromosome 2:233763993 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs61135950, rs34902870

This variation has 20 HGVS names - click the plus to show

2:g.233763993G>T
ENST00000373445.1:c.856-3041G>T
ENST00000305139.9:c.862-3041G>T
ENST00000373409.6:c.868-3041G>T
ENST00000482026.4:c.868-3041G>T
ENST00000373424.4:c.61-3041G>T
ENST00000446481.5:c.61-3041G>T
ENST00000373426.3:c.856-3041G>T
ENST00000450233.1:c.868-3041G>T
ENST00000360418.4:c.864+2842G>T
ENST00000609767.2:c.868-3041G>T
ENST00000373414.3:c.868-3041G>T
ENST00000305208.8:c.864+2842G>T
ENST00000406651.1:c.61-3041G>T
ENST00000373450.4:c.856-3041G>T
ENST00000344644.8:c.856-3041G>T
ENST00000354728.4:c.856-3041G>T
ENST00000484784.2:c.*238-3041G>T
LRG_733:g.8721G>T
LRG_733t1:c.864+2842G>T

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

About this variant

This variant overlaps 19 transcripts, has 2379 individual genotypes, is associated with 6 phenotypes and is mentioned in 13 citations.

Variation displays