Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 1:75127234 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

1:g.75127234C>G

About this variant

This variant overlaps 4 transcripts and has 270 sample genotypes.

Variant displays