Original source

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

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

Chromosome 9:114796423 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61572525

This variation has 2 HGVS names - click the plus to show

9:g.114796423C>T
ENST00000374045.4:c.211-2855G>A

This variation has assays on 14 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4874 individual genotypes, is associated with 3 phenotypes and is mentioned in 22 citations.

Variation displays