Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.16 (C)
Location

Chromosome 15:74035865 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM097806

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 36 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 40 transcripts and has 2845 sample genotypes.

Variant displays