Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.03 (C)
Location

Chromosome 1:99848214 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.99848214T>C

About this variant

This variant overlaps 6 transcripts and has 2504 sample genotypes.

Variant displays