rs786205488

Orientation

plus

Stabilized

plus

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

Make rs786205488(C;T)

Make rs786205488(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

64007107

Gene

SYNE2

is a	snp
is	mentioned by
dbSNP	rs786205488
dbSNP (classic)	rs786205488
ClinGen	rs786205488
ebi	rs786205488
HLI	rs786205488
Exac	rs786205488
Gnomad	rs786205488
Varsome	rs786205488
LitVar	rs786205488
Map	rs786205488
PheGenI	rs786205488
Biobank	rs786205488
1000 genomes	rs786205488
hgdp	rs786205488
ensembl	rs786205488
geneview	rs786205488
scholar	rs786205488
google	rs786205488
pharmgkb	rs786205488
gwascentral	rs786205488
openSNP	rs786205488
23andMe	rs786205488
SNPshot	rs786205488
SNPdbe	rs786205488
MSV3d	rs786205488
GWAS Ctlg	rs786205488

Max Magnitude

0

ClinVar
Risk	rs786205488(T;T)
Alt	rs786205488(T;T)
Reference	Rs786205488(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SYNE2
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.64473825C>T
CLNSRC
CLNACC	RCV000171223.1,