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rs199660234

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199660234(C;G)
Make rs199660234(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672249
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs199660234
ebirs199660234
HLIrs199660234
Exacrs199660234
Varsomers199660234
Maprs199660234
PheGenIrs199660234
hapmaprs199660234
1000 genomesrs199660234
hgdprs199660234
ensemblrs199660234
gopubmedrs199660234
geneviewrs199660234
scholarrs199660234
googlers199660234
pharmgkbrs199660234
gwascentralrs199660234
openSNPrs199660234
23andMers199660234
23andMe allrs199660234
SNP Nexus

SNPshotrs199660234
SNPdbers199660234
MSV3drs199660234
GWAS Ctlgrs199660234
Max Magnitude0
ClinVar
Risk rs199660234(G,T;G,T)
Alt rs199660234(G,T;G,T)
Reference rs199660234(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713741C>G
CLNSRC
CLNACC RCV000197867.1,