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rs104895089

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 Carrier of a familial mediterranean fever mutation
Make rs104895089(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position3243449
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895089
ebirs104895089
HLIrs104895089
Exacrs104895089
Varsomers104895089
Maprs104895089
PheGenIrs104895089
hapmaprs104895089
1000 genomesrs104895089
hgdprs104895089
ensemblrs104895089
gopubmedrs104895089
geneviewrs104895089
scholarrs104895089
googlers104895089
pharmgkbrs104895089
gwascentralrs104895089
openSNPrs104895089
23andMers104895089
23andMe allrs104895089
SNP Nexus

SNPshotrs104895089
SNPdbers104895089
MSV3drs104895089
GWAS Ctlgrs104895089
Max Magnitude3
ClinVar
Risk rs104895089(C;C)
Alt rs104895089(C;C)
Reference rs104895089(A;A)
Significance Untested
Disease Familial Mediterranean fever
Variation info
Gene MEFV
CLNDBN Familial Mediterranean fever
Reversed 1
HGVS NC_000016.9:g.3293449T>G
CLNSRC
CLNACC RCV000083732.1,