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rs1064793237

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position42721813
GenePRPH2
is asnp
is mentioned by
dbSNPrs1064793237
dbSNP (old)rs1064793237
ClinGenrs1064793237
ebirs1064793237
HLIrs1064793237
Exacrs1064793237
Gnomadrs1064793237
Varsomers1064793237
Maprs1064793237
PheGenIrs1064793237
Biobankrs1064793237
1000 genomesrs1064793237
hgdprs1064793237
ensemblrs1064793237
gopubmedrs1064793237
geneviewrs1064793237
scholarrs1064793237
googlers1064793237
pharmgkbrs1064793237
gwascentralrs1064793237
openSNPrs1064793237
23andMers1064793237
23andMe allrs1064793237
SNPshotrs1064793237
SNPdbers1064793237
MSV3drs1064793237
GWAS Ctlgrs1064793237
Max Magnitude0
ClinVar
Risk rs1064793237(C;C)
Alt rs1064793237(C;C)
Reference Rs1064793237(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRPH2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.42689551C>G
CLNSRC
CLNACC RCV000479816.1,