Have questions? Visit https://www.reddit.com/r/SNPedia

rs764125009

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764125009(G;T)
Make rs764125009(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position105601349
GeneFKTN
is asnp
is mentioned by
dbSNPrs764125009
ebirs764125009
HLIrs764125009
Exacrs764125009
Varsomers764125009
Maprs764125009
PheGenIrs764125009
hapmaprs764125009
1000 genomesrs764125009
hgdprs764125009
ensemblrs764125009
gopubmedrs764125009
geneviewrs764125009
scholarrs764125009
googlers764125009
pharmgkbrs764125009
gwascentralrs764125009
openSNPrs764125009
23andMers764125009
23andMe allrs764125009
SNP Nexus

SNPshotrs764125009
SNPdbers764125009
MSV3drs764125009
GWAS Ctlgrs764125009
Max Magnitude0
ClinVar
Risk rs764125009(C,T;C,T)
Alt rs764125009(C,T;C,T)
Reference rs764125009(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FKTN
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.108363630G>T
CLNSRC
CLNACC RCV000224731.1,