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rs201070132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201070132(C;T)
Make rs201070132(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66993288
GeneSBDS
is asnp
is mentioned by
dbSNPrs201070132
dbSNP (classic)rs201070132
ClinGenrs201070132
ebirs201070132
HLIrs201070132
Exacrs201070132
Gnomadrs201070132
Varsomers201070132
LitVarrs201070132
Maprs201070132
PheGenIrs201070132
Biobankrs201070132
1000 genomesrs201070132
hgdprs201070132
ensemblrs201070132
geneviewrs201070132
scholarrs201070132
googlers201070132
pharmgkbrs201070132
gwascentralrs201070132
openSNPrs201070132
23andMers201070132
23andMe allrs201070132
SNPshotrs201070132
SNPdbers201070132
MSV3drs201070132
GWAS Ctlgrs201070132
Max Magnitude0
ClinVar
Risk rs201070132(T;T)
Alt rs201070132(T;T)
Reference Rs201070132(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SBDS
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.66458275C>T
CLNSRC
CLNACC RCV000414254.1,