Have questions? Visit https://www.reddit.com/r/SNPedia

rs104895366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104895366(A;T)
Make rs104895366(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position109590802
GeneMVK
is asnp
is mentioned by
dbSNPrs104895366
dbSNP (classic)rs104895366
ClinGenrs104895366
ebirs104895366
HLIrs104895366
Exacrs104895366
Gnomadrs104895366
Varsomers104895366
LitVarrs104895366
Maprs104895366
PheGenIrs104895366
Biobankrs104895366
1000 genomesrs104895366
hgdprs104895366
ensemblrs104895366
geneviewrs104895366
scholarrs104895366
googlers104895366
pharmgkbrs104895366
gwascentralrs104895366
openSNPrs104895366
23andMers104895366
23andMe allrs104895366
SNPshotrs104895366
SNPdbers104895366
MSV3drs104895366
GWAS Ctlgrs104895366
Max Magnitude0
ClinVar
Risk rs104895366(T;T)
Alt rs104895366(T;T)
Reference Rs104895366(A;A)
Significance Pathogenic
Disease Hyperimmunoglobulin D with periodic fever not provided
Variation info
Gene MVK
CLNDBN Hyperimmunoglobulin D with periodic fever not provided
Reversed 0
HGVS NC_000012.11:g.110028607A>T
CLNSRC
CLNACC RCV000083864.1, RCV000480950.1,