rs875989885

Orientation

minus

Stabilized

minus

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

Make rs875989885(C;T)

Make rs875989885(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

133555706

Gene

SYCE1

is a	snp
is	mentioned by
dbSNP	rs875989885
dbSNP (classic)	rs875989885
ClinGen	rs875989885
ebi	rs875989885
HLI	rs875989885
Exac	rs875989885
Gnomad	rs875989885
Varsome	rs875989885
LitVar	rs875989885
Map	rs875989885
PheGenI	rs875989885
Biobank	rs875989885
1000 genomes	rs875989885
hgdp	rs875989885
ensembl	rs875989885
geneview	rs875989885
scholar	rs875989885
google	rs875989885
pharmgkb	rs875989885
gwascentral	rs875989885
openSNP	rs875989885
23andMe	rs875989885
SNPshot	rs875989885
SNPdbe	rs875989885
MSV3d	rs875989885
GWAS Ctlg	rs875989885

Max Magnitude

0

ClinVar
Risk	rs875989885(T;T)
Alt	rs875989885(T;T)
Reference	Rs875989885(C;C)
Significance	Pathogenic
Disease	Premature ovarian failure 12
Variation	info
Gene	SYCE1
CLNDBN	Premature ovarian failure 12
Reversed	1
HGVS	NC_000010.10:g.135369210G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000211464.1,