Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.02 (G)
Location

Chromosome 1:186674636 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM024574

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 2962 sample genotypes and is mentioned in 3 citations.

Variant displays