Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 10:37952139 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 5 synonyms - click the plus to show

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

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2686 sample genotypes and is mentioned in 1 citation.

Variant displays