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rs144499152

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs144499152(C;C)
Make rs144499152(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206771211
GeneFASTKD2
is asnp
is mentioned by
dbSNPrs144499152
ebirs144499152
HLIrs144499152
Exacrs144499152
Varsomers144499152
Maprs144499152
PheGenIrs144499152
hapmaprs144499152
1000 genomesrs144499152
hgdprs144499152
ensemblrs144499152
gopubmedrs144499152
geneviewrs144499152
scholarrs144499152
googlers144499152
pharmgkbrs144499152
gwascentralrs144499152
openSNPrs144499152
23andMers144499152
23andMe allrs144499152
SNP Nexus

SNPshotrs144499152
SNPdbers144499152
MSV3drs144499152
GWAS Ctlgrs144499152
Max Magnitude0
ClinVar
Risk rs144499152(C;C)
Alt rs144499152(C;C)
Reference rs144499152(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FASTKD2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.207635935T>C
CLNSRC
CLNACC RCV000199763.2,