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rs1064797182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome14
Position21325829
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs1064797182
dbSNP (old)rs1064797182
ClinGenrs1064797182
ebirs1064797182
HLIrs1064797182
Exacrs1064797182
Gnomadrs1064797182
Varsomers1064797182
Maprs1064797182
PheGenIrs1064797182
Biobankrs1064797182
1000 genomesrs1064797182
hgdprs1064797182
ensemblrs1064797182
gopubmedrs1064797182
geneviewrs1064797182
scholarrs1064797182
googlers1064797182
pharmgkbrs1064797182
gwascentralrs1064797182
openSNPrs1064797182
23andMers1064797182
23andMe allrs1064797182
SNPshotrs1064797182
SNPdbers1064797182
MSV3drs1064797182
GWAS Ctlgrs1064797182
Max Magnitude0
ClinVar
Risk rs1064797182(G;G)
Alt rs1064797182(G;G)
Reference Rs1064797182(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGRIP1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.21793988A>G
CLNSRC
CLNACC RCV000487634.1,