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rs1057518333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518333(A;A)
Make rs1057518333(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position100393759
GeneLOC102724406, SIM1
is asnp
is mentioned by
dbSNPrs1057518333
dbSNP (old)rs1057518333
ClinGenrs1057518333
ebirs1057518333
HLIrs1057518333
Exacrs1057518333
Gnomadrs1057518333
Varsomers1057518333
Maprs1057518333
PheGenIrs1057518333
Biobankrs1057518333
1000 genomesrs1057518333
hgdprs1057518333
ensemblrs1057518333
gopubmedrs1057518333
geneviewrs1057518333
scholarrs1057518333
googlers1057518333
pharmgkbrs1057518333
gwascentralrs1057518333
openSNPrs1057518333
23andMers1057518333
23andMe allrs1057518333
SNPshotrs1057518333
SNPdbers1057518333
MSV3drs1057518333
GWAS Ctlgrs1057518333
Max Magnitude0
ClinVar
Risk rs1057518333(A;A)
Alt rs1057518333(A;A)
Reference Rs1057518333(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SIM1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.100841635G>T
CLNSRC
CLNACC RCV000414358.1,