Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.17 (C)
Location

Chromosome 10:100193948 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17880376, rs56743359

HGVS names

This variant has 4 HGVS names - Hide

10:g.100193948A>C
ENST00000588656.1:n.96+36T>G
ENST00000590930.5:n.1995T>G
ENST00000370397.7:c.1974+36T>G

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4010 sample genotypes and is mentioned in 4 citations.

Variant displays