Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.36 (C)
Location

Chromosome 17:63918844 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR031006

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58303360

HGVS name

17:g.63918844T>C

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2512 sample genotypes and is mentioned in 1 citation.

Variant displays