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rs104895098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104895098(C;G)
Make rs104895098(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position3243423
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895098
dbSNP (old)rs104895098
ClinGenrs104895098
ebirs104895098
HLIrs104895098
Exacrs104895098
Gnomadrs104895098
Varsomers104895098
Maprs104895098
PheGenIrs104895098
Biobankrs104895098
1000 genomesrs104895098
hgdprs104895098
ensemblrs104895098
gopubmedrs104895098
geneviewrs104895098
scholarrs104895098
googlers104895098
pharmgkbrs104895098
gwascentralrs104895098
openSNPrs104895098
23andMers104895098
23andMe allrs104895098
SNP Nexus

SNPshotrs104895098
SNPdbers104895098
MSV3drs104895098
GWAS Ctlgrs104895098
Max Magnitude0
ClinVar
Risk rs104895098(G;G)
Alt rs104895098(G;G)
Reference Rs104895098(C;C)
Significance Pathogenic
Disease Familial Mediterranean fever
Variation info
Gene MEFV
CLNDBN Familial Mediterranean fever
Reversed 1
HGVS NC_000016.9:g.3293423G>C
CLNSRC
CLNACC RCV000083736.1,