Original source

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

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

Chromosome 1:102876425 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

1:g.102876425T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts and has 2505 sample genotypes.

Variant displays