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: 0.08 (T)
Location

Chromosome 11:117661016 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57276883, rs56525925

This variation has 3 HGVS names - click the plus to show

11:g.117661016C>T
ENST00000527706.2:c.102+119739G>A
ENST00000321322.6:c.691+115775G>A

This variation has assays on 5 chips - click the plus to show

Variation displays