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rs786204108

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204108(C;C)
Make rs786204108(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position100626866
GeneLOC105375428, TFR2
is asnp
is mentioned by
dbSNPrs786204108
ebirs786204108
HLIrs786204108
Exacrs786204108
Varsomers786204108
Maprs786204108
PheGenIrs786204108
hapmaprs786204108
1000 genomesrs786204108
hgdprs786204108
ensemblrs786204108
gopubmedrs786204108
geneviewrs786204108
scholarrs786204108
googlers786204108
pharmgkbrs786204108
gwascentralrs786204108
openSNPrs786204108
23andMers786204108
23andMe allrs786204108
SNP Nexus

SNPshotrs786204108
SNPdbers786204108
MSV3drs786204108
GWAS Ctlgrs786204108
Max Magnitude0
ClinVar
Risk rs786204108(C;C)
Alt rs786204108(C;C)
Reference rs786204108(G;G)
Significance Probable-Pathogenic
Disease Hemochromatosis type 1
Variation info
Gene TFR2
CLNDBN Hemochromatosis type 1
Reversed 1
HGVS NC_000007.13:g.100224489C>G
CLNSRC
CLNACC RCV000168040.1,