rs185436876

Orientation

plus

Stabilized

plus

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

Make rs185436876(C;T)

Make rs185436876(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

161984849

Gene

OLFML2B

is a	snp
is	mentioned by
dbSNP	rs185436876
dbSNP (classic)	rs185436876
ClinGen	rs185436876
ebi	rs185436876
HLI	rs185436876
Exac	rs185436876
Gnomad	rs185436876
Varsome	rs185436876
LitVar	rs185436876
Map	rs185436876
PheGenI	rs185436876
Biobank	rs185436876
1000 genomes	rs185436876
hgdp	rs185436876
ensembl	rs185436876
geneview	rs185436876
scholar	rs185436876
google	rs185436876
pharmgkb	rs185436876
gwascentral	rs185436876
openSNP	rs185436876
23andMe	rs185436876
SNPshot	rs185436876
SNPdbe	rs185436876
MSV3d	rs185436876
GWAS Ctlg	rs185436876

Max Magnitude

0

ClinVar
Risk	rs185436876(A;A) rs185436876(T;T)
Alt	rs185436876(A;A) rs185436876(T;T)
Reference	Rs185436876(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OLFML2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.161954639C>T
CLNSRC	München/ Helmholtz Zentrum München
CLNACC	RCV000201204.1,