Original source

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

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

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

Co-located variant

HGMD-PUBLIC CM962768

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 10 HGVS names - 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