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rs879254316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879254316(A;A)
Make rs879254316(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position149041411
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs879254316
dbSNP (classic)rs879254316
ClinGenrs879254316
ebirs879254316
HLIrs879254316
Exacrs879254316
Gnomadrs879254316
Varsomers879254316
LitVarrs879254316
Maprs879254316
PheGenIrs879254316
Biobankrs879254316
1000 genomesrs879254316
hgdprs879254316
ensemblrs879254316
geneviewrs879254316
scholarrs879254316
googlers879254316
pharmgkbrs879254316
gwascentralrs879254316
openSNPrs879254316
23andMers879254316
SNPshotrs879254316
SNPdbers879254316
MSV3drs879254316
GWAS Ctlgrs879254316
Max Magnitude0
ClinVar
Risk rs879254316(A;A)
Alt rs879254316(A;A)
Reference Rs879254316(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.148420974C>T
CLNSRC
CLNACC RCV000236994.1,