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rs797044561

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044561(C;C)
Make rs797044561(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position46837102
GeneRP2
is asnp
is mentioned by
dbSNPrs797044561
ebirs797044561
HLIrs797044561
Exacrs797044561
Varsomers797044561
Maprs797044561
PheGenIrs797044561
hapmaprs797044561
1000 genomesrs797044561
hgdprs797044561
ensemblrs797044561
gopubmedrs797044561
geneviewrs797044561
scholarrs797044561
googlers797044561
pharmgkbrs797044561
gwascentralrs797044561
openSNPrs797044561
23andMers797044561
23andMe allrs797044561
SNP Nexus

SNPshotrs797044561
SNPdbers797044561
MSV3drs797044561
GWAS Ctlgrs797044561
Max Magnitude0
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,