rs538881762

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs538881762(C;T)

Make rs538881762(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

78726217

Gene	LOC107984422, TENM4

is a	snp
is	mentioned by
dbSNP	rs538881762
dbSNP (classic)	rs538881762
ClinGen	rs538881762
ebi	rs538881762
HLI	rs538881762
Exac	rs538881762
Gnomad	rs538881762
Varsome	rs538881762
LitVar	rs538881762
Map	rs538881762
PheGenI	rs538881762
Biobank	rs538881762
1000 genomes	rs538881762
hgdp	rs538881762
ensembl	rs538881762
geneview	rs538881762
scholar	rs538881762
google	rs538881762
pharmgkb	rs538881762
gwascentral	rs538881762
openSNP	rs538881762
23andMe	rs538881762
SNPshot	rs538881762
SNPdbe	rs538881762
MSV3d	rs538881762
GWAS Ctlg	rs538881762

Max Magnitude

0

ClinVar
Risk	rs538881762(T;T)
Alt	rs538881762(T;T)
Reference	Rs538881762(C;C)
Significance	Pathogenic
Disease	Tremor
Variation	info
Gene	TENM4
CLNDBN	Tremor, hereditary essential, 5
Reversed	0
HGVS	NC_000011.9:g.78437262C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000203554.1,