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rs104895103

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 Carrier of a familial mediterranean fever mutation
Make rs104895103(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position3254746
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895103
ebirs104895103
HLIrs104895103
Exacrs104895103
Varsomers104895103
Maprs104895103
PheGenIrs104895103
hapmaprs104895103
1000 genomesrs104895103
hgdprs104895103
ensemblrs104895103
gopubmedrs104895103
geneviewrs104895103
scholarrs104895103
googlers104895103
pharmgkbrs104895103
gwascentralrs104895103
openSNPrs104895103
23andMers104895103
23andMe allrs104895103
SNP Nexus

SNPshotrs104895103
SNPdbers104895103
MSV3drs104895103
GWAS Ctlgrs104895103
Max Magnitude3
ClinVar
Risk rs104895103(C,G;C,G)
Alt rs104895103(C,G;C,G)
Reference rs104895103(A;A)
Significance Pathogenic
Disease Familial Mediterranean fever not provided
Variation info
Gene MEFV
CLNDBN Familial Mediterranean fever not provided
Reversed 1
HGVS NC_000016.9:g.3304746T>G
CLNSRC
CLNACC RCV000083767.1, RCV000213178.1,