Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.23 (A)
Location

Chromosome 1:43337449 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR043164

Most severe consequence
 
Upstream gene variant
Evidence status

This variant has 2 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3814 sample genotypes.

Variant displays