rs763485258

Orientation

plus

Stabilized

plus

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

Make rs763485258(A;A)

Make rs763485258(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

78708470

Gene

TENM4

is a	snp
is	mentioned by
dbSNP	rs763485258
dbSNP (classic)	rs763485258
ClinGen	rs763485258
ebi	rs763485258
HLI	rs763485258
Exac	rs763485258
Gnomad	rs763485258
Varsome	rs763485258
LitVar	rs763485258
Map	rs763485258
PheGenI	rs763485258
Biobank	rs763485258
1000 genomes	rs763485258
hgdp	rs763485258
ensembl	rs763485258
geneview	rs763485258
scholar	rs763485258
google	rs763485258
pharmgkb	rs763485258
gwascentral	rs763485258
openSNP	rs763485258
23andMe	rs763485258
SNPshot	rs763485258
SNPdbe	rs763485258
MSV3d	rs763485258
GWAS Ctlg	rs763485258

Max Magnitude

0

ClinVar
Risk	rs763485258(A;A) rs763485258(T;T)
Alt	rs763485258(A;A) rs763485258(T;T)
Reference	Rs763485258(G;G)
Significance	Pathogenic
Disease	Tremor
Variation	info
Gene	TENM4
CLNDBN	Tremor, hereditary essential, 5
Reversed	0
HGVS	NC_000011.9:g.78419515G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000203504.1,