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: 0.15 (T)
Location

Chromosome 11:126231037 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61401095, rs58255041

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

11:g.126231037C>T
ENST00000528985.3:c.-144+1744C>T
ENST00000533050.3:c.-8+1744C>T
ENST00000530043.3:c.-8+1701C>T
ENST00000525728.3:n.134+1744C>T
ENST00000525338.1:c.-8+1744C>T
ENST00000360194.6:c.-7-3958C>T
ENST00000527247.3:n.70+1744C>T
ENST00000529731.3:c.-7-3958C>T

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

Variation displays