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rs1045409136

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position235489269
GeneB3GALNT2
is asnp
is mentioned by
dbSNPrs1045409136
dbSNP (old)rs1045409136
ClinGenrs1045409136
ebirs1045409136
HLIrs1045409136
Exacrs1045409136
Gnomadrs1045409136
Varsomers1045409136
Maprs1045409136
PheGenIrs1045409136
Biobankrs1045409136
1000 genomesrs1045409136
hgdprs1045409136
ensemblrs1045409136
gopubmedrs1045409136
geneviewrs1045409136
scholarrs1045409136
googlers1045409136
pharmgkbrs1045409136
gwascentralrs1045409136
openSNPrs1045409136
23andMers1045409136
23andMe allrs1045409136
SNPshotrs1045409136
SNPdbers1045409136
MSV3drs1045409136
GWAS Ctlgrs1045409136
Max Magnitude0
ClinVar
Risk rs1045409136(T;T)
Alt rs1045409136(T;T)
Reference Rs1045409136(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene B3GALNT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.235652574C>T
CLNSRC
CLNACC RCV000479796.1,