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rs1057518187

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518187(A;A)
Make rs1057518187(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position5693315
GeneSOX11
is asnp
is mentioned by
dbSNPrs1057518187
dbSNP (old)rs1057518187
ClinGenrs1057518187
ebirs1057518187
HLIrs1057518187
Exacrs1057518187
Gnomadrs1057518187
Varsomers1057518187
Maprs1057518187
PheGenIrs1057518187
Biobankrs1057518187
1000 genomesrs1057518187
hgdprs1057518187
ensemblrs1057518187
gopubmedrs1057518187
geneviewrs1057518187
scholarrs1057518187
googlers1057518187
pharmgkbrs1057518187
gwascentralrs1057518187
openSNPrs1057518187
23andMers1057518187
23andMe allrs1057518187
SNPshotrs1057518187
SNPdbers1057518187
MSV3drs1057518187
GWAS Ctlgrs1057518187
Max Magnitude0
ClinVar
Risk rs1057518187(A;A)
Alt rs1057518187(A;A)
Reference Rs1057518187(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SOX11
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.5833447C>A
CLNSRC
CLNACC RCV000414399.1,