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rs104895311

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104895311(A;A)
Make rs104895311(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position109586058
GeneMVK
is asnp
is mentioned by
dbSNPrs104895311
ebirs104895311
HLIrs104895311
Exacrs104895311
Varsomers104895311
Maprs104895311
PheGenIrs104895311
hapmaprs104895311
1000 genomesrs104895311
hgdprs104895311
ensemblrs104895311
gopubmedrs104895311
geneviewrs104895311
scholarrs104895311
googlers104895311
pharmgkbrs104895311
gwascentralrs104895311
openSNPrs104895311
23andMers104895311
23andMe allrs104895311
SNP Nexus

SNPshotrs104895311
SNPdbers104895311
MSV3drs104895311
GWAS Ctlgrs104895311
Max Magnitude0
ClinVar
Risk rs104895311(A;A)
Alt rs104895311(A;A)
Reference Rs104895311(G;G)
Significance Pathogenic
Disease Hyperimmunoglobulin D with periodic fever
Variation info
Gene MVK
CLNDBN Hyperimmunoglobulin D with periodic fever
Reversed 0
HGVS NC_000012.11:g.110023863G>A
CLNSRC
CLNACC RCV000083849.2,