rs774225566

Orientation

plus

Stabilized

plus

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

Make rs774225566(C;C)

Make rs774225566(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

133558953

Gene

SYCE1

is a	snp
is	mentioned by
dbSNP	rs774225566
dbSNP (classic)	rs774225566
ClinGen	rs774225566
ebi	rs774225566
HLI	rs774225566
Exac	rs774225566
Gnomad	rs774225566
Varsome	rs774225566
LitVar	rs774225566
Map	rs774225566
PheGenI	rs774225566
Biobank	rs774225566
1000 genomes	rs774225566
hgdp	rs774225566
ensembl	rs774225566
geneview	rs774225566
scholar	rs774225566
google	rs774225566
pharmgkb	rs774225566
gwascentral	rs774225566
openSNP	rs774225566
23andMe	rs774225566
SNPshot	rs774225566
SNPdbe	rs774225566
MSV3d	rs774225566
GWAS Ctlg	rs774225566

Max Magnitude

0

ClinVar
Risk	rs774225566(C;C)
Alt	rs774225566(C;C)
Reference	Rs774225566(T;T)
Significance	Pathogenic
Disease	Spermatogenic failure 15
Variation	info
Gene	SYCE1
CLNDBN	Spermatogenic failure 15
Reversed	0
HGVS	NC_000010.10:g.135372457T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000211704.2,