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rs1044894207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position43776268
GeneCSTB
is asnp
is mentioned by
dbSNPrs1044894207
dbSNP (old)rs1044894207
ClinGenrs1044894207
ebirs1044894207
HLIrs1044894207
Exacrs1044894207
Gnomadrs1044894207
Varsomers1044894207
Maprs1044894207
PheGenIrs1044894207
Biobankrs1044894207
1000 genomesrs1044894207
hgdprs1044894207
ensemblrs1044894207
gopubmedrs1044894207
geneviewrs1044894207
scholarrs1044894207
googlers1044894207
pharmgkbrs1044894207
gwascentralrs1044894207
openSNPrs1044894207
23andMers1044894207
23andMe allrs1044894207
SNPshotrs1044894207
SNPdbers1044894207
MSV3drs1044894207
GWAS Ctlgrs1044894207
Max Magnitude0
ClinVar
Risk rs1044894207(AT;AT)
Alt rs1044894207(AT;AT)
Reference Rs1044894207(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CSTB
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.45196149_45196150insAT
CLNSRC
CLNACC RCV000485922.1,