Original source

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

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

Chromosome 6:34427896 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

6:g.34427896C>T

About this variant

This variant overlaps 8 transcripts and has 2508 sample genotypes.

Variant displays