rs201659924

Orientation

plus

Stabilized

plus

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

Make rs201659924(C;T)

Make rs201659924(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

47607033

Gene

SYN1

is a	snp
is	mentioned by
dbSNP	rs201659924
dbSNP (classic)	rs201659924
ClinGen	rs201659924
ebi	rs201659924
HLI	rs201659924
Exac	rs201659924
Gnomad	rs201659924
Varsome	rs201659924
LitVar	rs201659924
Map	rs201659924
PheGenI	rs201659924
Biobank	rs201659924
1000 genomes	rs201659924
hgdp	rs201659924
ensembl	rs201659924
geneview	rs201659924
scholar	rs201659924
google	rs201659924
pharmgkb	rs201659924
gwascentral	rs201659924
openSNP	rs201659924
23andMe	rs201659924
SNPshot	rs201659924
SNPdbe	rs201659924
MSV3d	rs201659924
GWAS Ctlg	rs201659924

Max Magnitude

0

ClinVar
Risk	rs201659924(T;T)
Alt	rs201659924(T;T)
Reference	Rs201659924(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SYN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.47466432C>T
CLNSRC
CLNACC	RCV000189665.2,