Rs104895085

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104895085(A;A)
Make rs104895085(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position3243529
GeneMEFV
is asnp
is mentioned by
dbSNPrs104895085
Exacrs104895085
PheGenIrs104895085
nextbiors104895085
hapmaprs104895085
1000 genomesrs104895085
hgdprs104895085
ensemblrs104895085
gopubmedrs104895085
geneviewrs104895085
scholarrs104895085
googlers104895085
pharmgkbrs104895085
gwascentralrs104895085
openSNPrs104895085
23andMers104895085
23andMe allrs104895085
SNP Nexus

SNPshotrs104895085
SNPdbers104895085
MSV3drs104895085
Max Magnitude0
OMIM608107
Desc
Variant0016
Relatedalso
ClinVar
Risk rs104895085(A;A)
Alt rs104895085(A;A)
Reference rs104895085(G;G)
Significance Pathogenic
Disease Familial Mediterranean fever
Variation info
Gene MEFV
CLNDBN Familial Mediterranean fever
Reversed 1
HGVS NC_000016.9:g.3293529C>T
CLNSRC OMIM Allelic Variant Unité médicale des maladies autoinflammatoires
CLNACC RCV000002662.1,