Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 8:103441608 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs35443348

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts and has 2542 sample genotypes.

Variant displays