Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 4 HGVS names - click the plus to show

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

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

About this variant

This variant overlaps 5 transcripts, has 2871 sample genotypes and is mentioned in 4 citations.

Variant displays