rs797044561

Orientation

plus

Stabilized

plus

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

Make rs797044561(C;C)

Make rs797044561(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

46837102

Gene

RP2

is a	snp
is	mentioned by
dbSNP	rs797044561
dbSNP (classic)	rs797044561
ClinGen	rs797044561
ebi	rs797044561
HLI	rs797044561
Exac	rs797044561
Gnomad	rs797044561
Varsome	rs797044561
LitVar	rs797044561
Map	rs797044561
PheGenI	rs797044561
Biobank	rs797044561
1000 genomes	rs797044561
hgdp	rs797044561
ensembl	rs797044561
geneview	rs797044561
scholar	rs797044561
google	rs797044561
pharmgkb	rs797044561
gwascentral	rs797044561
openSNP	rs797044561
23andMe	rs797044561
SNPshot	rs797044561
SNPdbe	rs797044561
MSV3d	rs797044561
GWAS Ctlg	rs797044561

Max Magnitude

0

ClinVar
Risk	rs797044561(C;C)
Alt	rs797044561(C;C)
Reference	Rs797044561(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.46696537T>C
CLNSRC
CLNACC	RCV000171435.1,