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rs138211175

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138211175(C;T)
Make rs138211175(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43058919
GeneCBS
is asnp
is mentioned by
dbSNPrs138211175
ebirs138211175
HLIrs138211175
Exacrs138211175
Varsomers138211175
Maprs138211175
PheGenIrs138211175
hapmaprs138211175
1000 genomesrs138211175
hgdprs138211175
ensemblrs138211175
gopubmedrs138211175
geneviewrs138211175
scholarrs138211175
googlers138211175
pharmgkbrs138211175
gwascentralrs138211175
openSNPrs138211175
23andMers138211175
23andMe allrs138211175
SNP Nexus

SNPshotrs138211175
SNPdbers138211175
MSV3drs138211175
GWAS Ctlgrs138211175
Max Magnitude0
ClinVar
Risk rs138211175(T;T)
Alt rs138211175(T;T)
Reference rs138211175(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44479029C>T
CLNSRC
CLNACC RCV000200590.1,