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rs1057519117

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519117(G;T)
Make rs1057519117(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position50459667
GeneSBF1
is asnp
is mentioned by
dbSNPrs1057519117
dbSNP (old)rs1057519117
ClinGenrs1057519117
ebirs1057519117
HLIrs1057519117
Exacrs1057519117
Gnomadrs1057519117
Varsomers1057519117
Maprs1057519117
PheGenIrs1057519117
Biobankrs1057519117
1000 genomesrs1057519117
hgdprs1057519117
ensemblrs1057519117
gopubmedrs1057519117
geneviewrs1057519117
scholarrs1057519117
googlers1057519117
pharmgkbrs1057519117
gwascentralrs1057519117
openSNPrs1057519117
23andMers1057519117
23andMe allrs1057519117
SNPshotrs1057519117
SNPdbers1057519117
MSV3drs1057519117
GWAS Ctlgrs1057519117
Max Magnitude0
ClinVar
Risk rs1057519117(T;T)
Alt rs1057519117(T;T)
Reference Rs1057519117(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SBF1
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.50898096C>A
CLNSRC
CLNACC RCV000415967.1,