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rs1057524681

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524681(A;A)
Make rs1057524681(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position216477129
GeneSMARCAL1
is asnp
is mentioned by
dbSNPrs1057524681
dbSNP (old)rs1057524681
ClinGenrs1057524681
ebirs1057524681
HLIrs1057524681
Exacrs1057524681
Gnomadrs1057524681
Varsomers1057524681
Maprs1057524681
PheGenIrs1057524681
Biobankrs1057524681
1000 genomesrs1057524681
hgdprs1057524681
ensemblrs1057524681
gopubmedrs1057524681
geneviewrs1057524681
scholarrs1057524681
googlers1057524681
pharmgkbrs1057524681
gwascentralrs1057524681
openSNPrs1057524681
23andMers1057524681
23andMe allrs1057524681
SNPshotrs1057524681
SNPdbers1057524681
MSV3drs1057524681
GWAS Ctlgrs1057524681
Max Magnitude0
ClinVar
Risk rs1057524681(A;A)
Alt rs1057524681(A;A)
Reference Rs1057524681(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMARCAL1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.217341852C>A
CLNSRC
CLNACC RCV000431974.1,