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rs759805984

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs759805984(A;A)
Make rs759805984(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99149213
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs759805984
ebirs759805984
HLIrs759805984
Exacrs759805984
Varsomers759805984
Maprs759805984
PheGenIrs759805984
hapmaprs759805984
1000 genomesrs759805984
hgdprs759805984
ensemblrs759805984
gopubmedrs759805984
geneviewrs759805984
scholarrs759805984
googlers759805984
pharmgkbrs759805984
gwascentralrs759805984
openSNPrs759805984
23andMers759805984
23andMe allrs759805984
SNP Nexus

SNPshotrs759805984
SNPdbers759805984
MSV3drs759805984
GWAS Ctlgrs759805984
Max Magnitude0
ClinVar
Risk rs759805984(A;A)
Alt rs759805984(A;A)
Reference rs759805984(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101911495T>C
CLNSRC
CLNACC RCV000198521.1,