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rs1064793000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position7462259
GeneARHGEF18
is asnp
is mentioned by
dbSNPrs1064793000
dbSNP (old)rs1064793000
ClinGenrs1064793000
ebirs1064793000
HLIrs1064793000
Exacrs1064793000
Gnomadrs1064793000
Varsomers1064793000
LitVarrs1064793000
Maprs1064793000
PheGenIrs1064793000
Biobankrs1064793000
1000 genomesrs1064793000
hgdprs1064793000
ensemblrs1064793000
gopubmedrs1064793000
geneviewrs1064793000
scholarrs1064793000
googlers1064793000
pharmgkbrs1064793000
gwascentralrs1064793000
openSNPrs1064793000
23andMers1064793000
23andMe allrs1064793000
SNPshotrs1064793000
SNPdbers1064793000
MSV3drs1064793000
GWAS Ctlgrs1064793000
Max Magnitude0
ClinVar
Risk rs1064793000(T;T)
Alt rs1064793000(T;T)
Reference Rs1064793000(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 78
Variation info
Gene ARHGEF18
CLNDBN Retinitis pigmentosa 78
Reversed 0
HGVS NC_000019.9:g.7527145C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477673.1,