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rs879254317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879254317(G;T)
Make rs879254317(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position149027244
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs879254317
dbSNP (classic)rs879254317
ClinGenrs879254317
ebirs879254317
HLIrs879254317
Exacrs879254317
Gnomadrs879254317
Varsomers879254317
LitVarrs879254317
Maprs879254317
PheGenIrs879254317
Biobankrs879254317
1000 genomesrs879254317
hgdprs879254317
ensemblrs879254317
geneviewrs879254317
scholarrs879254317
googlers879254317
pharmgkbrs879254317
gwascentralrs879254317
openSNPrs879254317
23andMers879254317
SNPshotrs879254317
SNPdbers879254317
MSV3drs879254317
GWAS Ctlgrs879254317
Max Magnitude0
ClinVar
Risk rs879254317(T;T)
Alt rs879254317(T;T)
Reference Rs879254317(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.148406807C>A
CLNSRC
CLNACC RCV000235715.1,