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rs1064797314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position149027835
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs1064797314
dbSNP (old)rs1064797314
ClinGenrs1064797314
ebirs1064797314
HLIrs1064797314
Exacrs1064797314
Gnomadrs1064797314
Varsomers1064797314
LitVarrs1064797314
Maprs1064797314
PheGenIrs1064797314
Biobankrs1064797314
1000 genomesrs1064797314
hgdprs1064797314
ensemblrs1064797314
gopubmedrs1064797314
geneviewrs1064797314
scholarrs1064797314
googlers1064797314
pharmgkbrs1064797314
gwascentralrs1064797314
openSNPrs1064797314
23andMers1064797314
23andMe allrs1064797314
SNPshotrs1064797314
SNPdbers1064797314
MSV3drs1064797314
GWAS Ctlgrs1064797314
Max Magnitude0
ClinVar
Risk rs1064797314(-;-)
Alt rs1064797314(-;-)
Reference Rs1064797314(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.148407398delC
CLNSRC
CLNACC RCV000488187.1,