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rs1064797235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position29702933
GeneC19orf12
is asnp
is mentioned by
dbSNPrs1064797235
dbSNP (classic)rs1064797235
ClinGenrs1064797235
ebirs1064797235
HLIrs1064797235
Exacrs1064797235
Gnomadrs1064797235
Varsomers1064797235
LitVarrs1064797235
Maprs1064797235
PheGenIrs1064797235
Biobankrs1064797235
1000 genomesrs1064797235
hgdprs1064797235
ensemblrs1064797235
geneviewrs1064797235
scholarrs1064797235
googlers1064797235
pharmgkbrs1064797235
gwascentralrs1064797235
openSNPrs1064797235
23andMers1064797235
23andMe allrs1064797235
SNPshotrs1064797235
SNPdbers1064797235
MSV3drs1064797235
GWAS Ctlgrs1064797235
Max Magnitude0
ClinVar
Risk rs1064797235(T;T)
Alt rs1064797235(T;T)
Reference Rs1064797235(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C19orf12
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.30193840G>A
CLNSRC
CLNACC RCV000488270.1,