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rs104895134

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104895134(C;G)
Make rs104895134(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position3254529
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895134
ebirs104895134
HLIrs104895134
Exacrs104895134
Varsomers104895134
Maprs104895134
PheGenIrs104895134
hapmaprs104895134
1000 genomesrs104895134
hgdprs104895134
ensemblrs104895134
gopubmedrs104895134
geneviewrs104895134
scholarrs104895134
googlers104895134
pharmgkbrs104895134
gwascentralrs104895134
openSNPrs104895134
23andMers104895134
23andMe allrs104895134
SNP Nexus

SNPshotrs104895134
SNPdbers104895134
MSV3drs104895134
GWAS Ctlgrs104895134
Max Magnitude0
ClinVar
Risk rs104895134(T;T)
Alt rs104895134(T;T)
Reference Rs104895134(C;C)
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.3304529G>C; NC_000016.9:g.3304529G>T
CLNSRC
CLNACC RCV000083782.1, RCV000256072.1,