Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 7:94427801 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM962768

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays