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rs755659290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs755659290(C;C)
Make rs755659290(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3249480
GeneMEFV
is asnp
is mentioned by
dbSNPrs755659290
dbSNP (classic)rs755659290
ClinGenrs755659290
ebirs755659290
HLIrs755659290
Exacrs755659290
Gnomadrs755659290
Varsomers755659290
LitVarrs755659290
Maprs755659290
PheGenIrs755659290
Biobankrs755659290
1000 genomesrs755659290
hgdprs755659290
ensemblrs755659290
geneviewrs755659290
scholarrs755659290
googlers755659290
pharmgkbrs755659290
gwascentralrs755659290
openSNPrs755659290
23andMers755659290
23andMe allrs755659290
SNPshotrs755659290
SNPdbers755659290
MSV3drs755659290
GWAS Ctlgrs755659290
Max Magnitude0
ClinVar
Risk rs755659290(C;C)
Alt rs755659290(C;C)
Reference Rs755659290(T;T)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene MEFV
CLNDBN Behcet's syndrome
Reversed 0
HGVS NC_000016.9:g.3299480T>C
CLNSRC
CLNACC RCV000416328.1,