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rs1064796712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Chromosome17
Position40637577
GeneSMARCE1
is asnp
is mentioned by
dbSNPrs1064796712
dbSNP (old)rs1064796712
ClinGenrs1064796712
ebirs1064796712
HLIrs1064796712
Exacrs1064796712
Gnomadrs1064796712
Varsomers1064796712
LitVarrs1064796712
Maprs1064796712
PheGenIrs1064796712
Biobankrs1064796712
1000 genomesrs1064796712
hgdprs1064796712
ensemblrs1064796712
gopubmedrs1064796712
geneviewrs1064796712
scholarrs1064796712
googlers1064796712
pharmgkbrs1064796712
gwascentralrs1064796712
openSNPrs1064796712
23andMers1064796712
23andMe allrs1064796712
SNPshotrs1064796712
SNPdbers1064796712
MSV3drs1064796712
GWAS Ctlgrs1064796712
Max Magnitude0
ClinVar
Risk rs1064796712(AA;AA)
Alt rs1064796712(AA;AA)
Reference Rs1064796712(TC;TC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCE1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.38793829_38793830delGAinsTT
CLNSRC
CLNACC RCV000486403.1,