Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.31 (T)
Location

Chromosome 2:233759924 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

2:g.233759924C>T
ENST00000373445.1:c.856-7110C>T
ENST00000373409.4:c.868-7110C>T
ENST00000305139.7:c.862-7110C>T
ENST00000482026.2:c.868-7110C>T
ENST00000446481.3:c.61-7110C>T
ENST00000373424.2:c.61-7110C>T
ENST00000373426.3:c.856-7110C>T
ENST00000450233.1:c.868-7110C>T
ENST00000609767.2:c.868-7110C>T
ENST00000373414.3:c.868-7110C>T
ENST00000406651.1:c.61-7110C>T
ENST00000344644.6:c.856-7110C>T
ENST00000373450.4:c.856-7110C>T
ENST00000354728.4:c.856-7110C>T
ENST00000484784.2:c.*238-7110C>T
LRG_733:g.4652C>T

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

Variation displays