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rs1057524798

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524798(A;G)
Make rs1057524798(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53380670
GeneSMC1A
is asnp
is mentioned by
dbSNPrs1057524798
dbSNP (old)rs1057524798
ClinGenrs1057524798
ebirs1057524798
HLIrs1057524798
Exacrs1057524798
Gnomadrs1057524798
Varsomers1057524798
Maprs1057524798
PheGenIrs1057524798
Biobankrs1057524798
1000 genomesrs1057524798
hgdprs1057524798
ensemblrs1057524798
gopubmedrs1057524798
geneviewrs1057524798
scholarrs1057524798
googlers1057524798
pharmgkbrs1057524798
gwascentralrs1057524798
openSNPrs1057524798
23andMers1057524798
23andMe allrs1057524798
SNPshotrs1057524798
SNPdbers1057524798
MSV3drs1057524798
GWAS Ctlgrs1057524798
Max Magnitude0
ClinVar
Risk rs1057524798(G;G)
Alt rs1057524798(G;G)
Reference Rs1057524798(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMC1A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53407591T>C
CLNSRC
CLNACC RCV000441064.1,