Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.18 (C)
Location

Chromosome 10:100216744 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Hide

10:g.100216744G>C
ENST00000370397.7:c.933+1251C>G

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 transcript, has 4401 sample genotypes and is mentioned in 5 citations.

Variant displays