Original source

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

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

Chromosome 10:74082499 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM062022

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 27237

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays