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rs370465985

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs370465985(C;C)
Make rs370465985(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position47260359
GeneSTIL
is asnp
is mentioned by
dbSNPrs370465985
ebirs370465985
HLIrs370465985
Exacrs370465985
Varsomers370465985
Maprs370465985
PheGenIrs370465985
hapmaprs370465985
1000 genomesrs370465985
hgdprs370465985
ensemblrs370465985
gopubmedrs370465985
geneviewrs370465985
scholarrs370465985
googlers370465985
pharmgkbrs370465985
gwascentralrs370465985
openSNPrs370465985
23andMers370465985
23andMe allrs370465985
SNP Nexus

SNPshotrs370465985
SNPdbers370465985
MSV3drs370465985
GWAS Ctlgrs370465985
Max Magnitude0
ClinVar
Risk rs370465985(C;C)
Alt rs370465985(C;C)
Reference rs370465985(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene STIL
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.47726031T>C
CLNSRC
CLNACC RCV000210584.1,