Original source

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

Alleles
A/C/G|Ancestral: G|Ambiguity code: V|MAF: 0.44 (A)
Location

Chromosome 7:100818628 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 18 transcripts, has 3731 sample genotypes and is mentioned in 1 citation.

Variant displays