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rs1064793002

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome19
Position7456408
GeneARHGEF18
is asnp
is mentioned by
dbSNPrs1064793002
dbSNP (old)rs1064793002
ClinGenrs1064793002
ebirs1064793002
HLIrs1064793002
Exacrs1064793002
Gnomadrs1064793002
Varsomers1064793002
Maprs1064793002
PheGenIrs1064793002
Biobankrs1064793002
1000 genomesrs1064793002
hgdprs1064793002
ensemblrs1064793002
gopubmedrs1064793002
geneviewrs1064793002
scholarrs1064793002
googlers1064793002
pharmgkbrs1064793002
gwascentralrs1064793002
openSNPrs1064793002
23andMers1064793002
23andMe allrs1064793002
SNPshotrs1064793002
SNPdbers1064793002
MSV3drs1064793002
GWAS Ctlgrs1064793002
Max Magnitude0
ClinVar
Risk rs1064793002(A;A)
Alt rs1064793002(A;A)
Reference Rs1064793002(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 78
Variation info
Gene ARHGEF18
CLNDBN Retinitis pigmentosa 78
Reversed 0
HGVS NC_000019.9:g.7521294G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000477671.1,