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rs760906097

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760906097(A;A)
Make rs760906097(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position37221459
GeneC5orf42
is asnp
is mentioned by
dbSNPrs760906097
ebirs760906097
HLIrs760906097
Exacrs760906097
Varsomers760906097
Maprs760906097
PheGenIrs760906097
hapmaprs760906097
1000 genomesrs760906097
hgdprs760906097
ensemblrs760906097
gopubmedrs760906097
geneviewrs760906097
scholarrs760906097
googlers760906097
pharmgkbrs760906097
gwascentralrs760906097
openSNPrs760906097
23andMers760906097
23andMe allrs760906097
SNP Nexus

SNPshotrs760906097
SNPdbers760906097
MSV3drs760906097
GWAS Ctlgrs760906097
Max Magnitude0
ClinVar
Risk rs760906097(A;A)
Alt rs760906097(A;A)
Reference rs760906097(G;G)
Significance Pathogenic
Disease Joubert syndrome 17
Variation info
Gene C5orf42
CLNDBN Joubert syndrome 17
Reversed 0
HGVS NC_000005.9:g.37221561G>A
CLNSRC
CLNACC RCV000201667.1,