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rs879254057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs879254057(-;-)
Make rs879254057(-;AG)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position149062966
GeneLOC255187, MIR584, SH3TC2
is asnp
is mentioned by
dbSNPrs879254057
dbSNP (classic)rs879254057
ClinGenrs879254057
ebirs879254057
HLIrs879254057
Exacrs879254057
Gnomadrs879254057
Varsomers879254057
LitVarrs879254057
Maprs879254057
PheGenIrs879254057
Biobankrs879254057
1000 genomesrs879254057
hgdprs879254057
ensemblrs879254057
geneviewrs879254057
scholarrs879254057
googlers879254057
pharmgkbrs879254057
gwascentralrs879254057
openSNPrs879254057
23andMers879254057
SNPshotrs879254057
SNPdbers879254057
MSV3drs879254057
GWAS Ctlgrs879254057
Max Magnitude0
ClinVar
Risk rs879254057(-;-)
Alt rs879254057(-;-)
Reference Rs879254057(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH3TC2 MIR584 LOC255187
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.148442529_148442530delCT
CLNSRC
CLNACC RCV000236888.1,