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rs1060499624

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499624(C;G)
Make rs1060499624(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position108765788
GeneRANBP2
is asnp
is mentioned by
dbSNPrs1060499624
dbSNP (old)rs1060499624
ClinGenrs1060499624
ebirs1060499624
HLIrs1060499624
Exacrs1060499624
Gnomadrs1060499624
Varsomers1060499624
Maprs1060499624
PheGenIrs1060499624
Biobankrs1060499624
1000 genomesrs1060499624
hgdprs1060499624
ensemblrs1060499624
gopubmedrs1060499624
geneviewrs1060499624
scholarrs1060499624
googlers1060499624
pharmgkbrs1060499624
gwascentralrs1060499624
openSNPrs1060499624
23andMers1060499624
23andMe allrs1060499624
SNPshotrs1060499624
SNPdbers1060499624
MSV3drs1060499624
GWAS Ctlgrs1060499624
Max Magnitude0
ClinVar
Risk rs1060499624(G;G)
Alt rs1060499624(G;G)
Reference Rs1060499624(C;C)
Significance Probable-Pathogenic
Disease Encephalopathy
Variation info
Gene RANBP2
CLNDBN Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed 0
HGVS NC_000002.11:g.109382244C>G
CLNSRC
CLNACC RCV000445625.1,