Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (T)
Location

Chromosome 11:126100932 (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.126100932C>T
ENST00000528985.1:c.-144+1744C>T
ENST00000533050.1:c.-8+1744C>T
ENST00000530043.1:c.-8+1701C>T
ENST00000525728.1:n.134+1744C>T
ENST00000525338.1:c.-8+1744C>T
ENST00000360194.4:c.-7-3958C>T
ENST00000527247.1:n.70+1744C>T
ENST00000529731.1:c.-7-3958C>T

This variation has assays on 6 chips - click the plus to show

Variation displays