Original source

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

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

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