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rs786205597

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205597(G;T)
Make rs786205597(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position105601293
GeneFKTN
is asnp
is mentioned by
dbSNPrs786205597
ebirs786205597
HLIrs786205597
Exacrs786205597
Varsomers786205597
Maprs786205597
PheGenIrs786205597
hapmaprs786205597
1000 genomesrs786205597
hgdprs786205597
ensemblrs786205597
gopubmedrs786205597
geneviewrs786205597
scholarrs786205597
googlers786205597
pharmgkbrs786205597
gwascentralrs786205597
openSNPrs786205597
23andMers786205597
23andMe allrs786205597
SNP Nexus

SNPshotrs786205597
SNPdbers786205597
MSV3drs786205597
GWAS Ctlgrs786205597
Max Magnitude0
ClinVar
Risk rs786205597(T;T)
Alt rs786205597(T;T)
Reference rs786205597(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FKTN
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.108363574G>T
CLNSRC
CLNACC RCV000171426.1,