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rs1064795632

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position24240684
GeneTINF2
is asnp
is mentioned by
dbSNPrs1064795632
dbSNP (old)rs1064795632
ClinGenrs1064795632
ebirs1064795632
HLIrs1064795632
Exacrs1064795632
Gnomadrs1064795632
Varsomers1064795632
Maprs1064795632
PheGenIrs1064795632
Biobankrs1064795632
1000 genomesrs1064795632
hgdprs1064795632
ensemblrs1064795632
gopubmedrs1064795632
geneviewrs1064795632
scholarrs1064795632
googlers1064795632
pharmgkbrs1064795632
gwascentralrs1064795632
openSNPrs1064795632
23andMers1064795632
23andMe allrs1064795632
SNPshotrs1064795632
SNPdbers1064795632
MSV3drs1064795632
GWAS Ctlgrs1064795632
Max Magnitude0
ClinVar
Risk rs1064795632(T;T)
Alt rs1064795632(T;T)
Reference Rs1064795632(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TINF2
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.24709890G>A
CLNSRC
CLNACC RCV000481021.1,