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rs1057519328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519328(C;G)
Make rs1057519328(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3249592
GeneMEFV
is asnp
is mentioned by
dbSNPrs1057519328
dbSNP (old)rs1057519328
ClinGenrs1057519328
ebirs1057519328
HLIrs1057519328
Exacrs1057519328
Gnomadrs1057519328
Varsomers1057519328
LitVarrs1057519328
Maprs1057519328
PheGenIrs1057519328
Biobankrs1057519328
1000 genomesrs1057519328
hgdprs1057519328
ensemblrs1057519328
gopubmedrs1057519328
geneviewrs1057519328
scholarrs1057519328
googlers1057519328
pharmgkbrs1057519328
gwascentralrs1057519328
openSNPrs1057519328
23andMers1057519328
23andMe allrs1057519328
SNPshotrs1057519328
SNPdbers1057519328
MSV3drs1057519328
GWAS Ctlgrs1057519328
Max Magnitude0
ClinVar
Risk rs1057519328(G;G)
Alt rs1057519328(G;G)
Reference Rs1057519328(C;C)
Significance Pathogenic
Disease Behcet's syndrome
Variation info
Gene MEFV
CLNDBN Behcet's syndrome
Reversed 1
HGVS NC_000016.9:g.3299592G>C
CLNSRC
CLNACC RCV000416346.1,