rs560525099

Orientation

plus

Stabilized

plus

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

Make rs560525099(C;T)

Make rs560525099(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

47447904

Gene

RAPSN

is a	snp
is	mentioned by
dbSNP	rs560525099
dbSNP (classic)	rs560525099
ClinGen	rs560525099
ebi	rs560525099
HLI	rs560525099
Exac	rs560525099
Gnomad	rs560525099
Varsome	rs560525099
LitVar	rs560525099
Map	rs560525099
PheGenI	rs560525099
Biobank	rs560525099
1000 genomes	rs560525099
hgdp	rs560525099
ensembl	rs560525099
geneview	rs560525099
scholar	rs560525099
google	rs560525099
pharmgkb	rs560525099
gwascentral	rs560525099
openSNP	rs560525099
23andMe	rs560525099
SNPshot	rs560525099
SNPdbe	rs560525099
MSV3d	rs560525099
GWAS Ctlg	rs560525099

Max Magnitude

0

ClinVar
Risk	rs560525099(T;T)
Alt	rs560525099(T;T)
Reference	Rs560525099(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RAPSN
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.47469456C>T
CLNSRC
CLNACC	RCV000432123.1,