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rs1057524761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524761(A;A)
Make rs1057524761(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position66714359
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs1057524761
dbSNP (old)rs1057524761
ClinGenrs1057524761
ebirs1057524761
HLIrs1057524761
Exacrs1057524761
Gnomadrs1057524761
Varsomers1057524761
Maprs1057524761
PheGenIrs1057524761
Biobankrs1057524761
1000 genomesrs1057524761
hgdprs1057524761
ensemblrs1057524761
gopubmedrs1057524761
geneviewrs1057524761
scholarrs1057524761
googlers1057524761
pharmgkbrs1057524761
gwascentralrs1057524761
openSNPrs1057524761
23andMers1057524761
23andMe allrs1057524761
SNPshotrs1057524761
SNPdbers1057524761
MSV3drs1057524761
GWAS Ctlgrs1057524761
Max Magnitude0
ClinVar
Risk rs1057524761(A;A)
Alt rs1057524761(A;A)
Reference Rs1057524761(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTBN2
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66481830C>T
CLNSRC
CLNACC RCV000423934.1,