rs767507908

Orientation

plus

Stabilized

plus

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

Make rs767507908(A;A)

Make rs767507908(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

47448072

Gene

RAPSN

is a	snp
is	mentioned by
dbSNP	rs767507908
dbSNP (classic)	rs767507908
ClinGen	rs767507908
ebi	rs767507908
HLI	rs767507908
Exac	rs767507908
Gnomad	rs767507908
Varsome	rs767507908
LitVar	rs767507908
Map	rs767507908
PheGenI	rs767507908
Biobank	rs767507908
1000 genomes	rs767507908
hgdp	rs767507908
ensembl	rs767507908
geneview	rs767507908
scholar	rs767507908
google	rs767507908
pharmgkb	rs767507908
gwascentral	rs767507908
openSNP	rs767507908
23andMe	rs767507908
SNPshot	rs767507908
SNPdbe	rs767507908
MSV3d	rs767507908
GWAS Ctlg	rs767507908

Max Magnitude

0

ClinVar
Risk	rs767507908(A;A)
Alt	rs767507908(A;A)
Reference	Rs767507908(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RAPSN
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.47469624G>A
CLNSRC
CLNACC	RCV000443235.1,