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rs863223962

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223962(C;T)
Make rs863223962(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206767375
GeneFASTKD2, MDH1B
is asnp
is mentioned by
dbSNPrs863223962
ebirs863223962
HLIrs863223962
Exacrs863223962
Varsomers863223962
Maprs863223962
PheGenIrs863223962
hapmaprs863223962
1000 genomesrs863223962
hgdprs863223962
ensemblrs863223962
gopubmedrs863223962
geneviewrs863223962
scholarrs863223962
googlers863223962
pharmgkbrs863223962
gwascentralrs863223962
openSNPrs863223962
23andMers863223962
23andMe allrs863223962
SNP Nexus

SNPshotrs863223962
SNPdbers863223962
MSV3drs863223962
GWAS Ctlgrs863223962
Max Magnitude0
ClinVar
Risk rs863223962(T;T)
Alt rs863223962(T;T)
Reference rs863223962(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FASTKD2 MDH1B
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.207632099C>T
CLNSRC
CLNACC RCV000198572.1,