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rs786205579

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205579(A;A)
Make rs786205579(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position42721838
GenePRPH2
is asnp
is mentioned by
dbSNPrs786205579
ebirs786205579
HLIrs786205579
Exacrs786205579
Varsomers786205579
Maprs786205579
PheGenIrs786205579
hapmaprs786205579
1000 genomesrs786205579
hgdprs786205579
ensemblrs786205579
gopubmedrs786205579
geneviewrs786205579
scholarrs786205579
googlers786205579
pharmgkbrs786205579
gwascentralrs786205579
openSNPrs786205579
23andMers786205579
23andMe allrs786205579
SNP Nexus

SNPshotrs786205579
SNPdbers786205579
MSV3drs786205579
GWAS Ctlgrs786205579
Max Magnitude0
ClinVar
Risk rs786205579(A;A)
Alt rs786205579(A;A)
Reference rs786205579(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRPH2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.42689576C>T
CLNSRC
CLNACC RCV000171395.1,