Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.50 (T)
Location

Chromosome 2:233757013 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR025220

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs57409706

This variation has 17 HGVS names - click the plus to show

2:g.233757013T>G
ENST00000373445.1:c.856-10021T>G
ENST00000373409.5:c.868-10021T>G
ENST00000305139.8:c.862-10021T>G
ENST00000482026.3:c.868-10021T>G
ENST00000446481.4:c.61-10021T>G
ENST00000373424.3:c.61-10021T>G
ENST00000373426.3:c.856-10021T>G
ENST00000450233.1:c.868-10021T>G
ENST00000609767.2:c.868-10021T>G
ENST00000373414.3:c.868-10021T>G
ENST00000406651.1:c.61-10021T>G
ENST00000373450.4:c.856-10021T>G
ENST00000344644.7:c.856-10021T>G
ENST00000354728.4:c.856-10021T>G
ENST00000484784.2:c.*238-10021T>G
LRG_733:g.1741T>G

This variation has assays on 7 chips - click the plus to show

Variation displays