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

rs34371500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs34371500(G;T)
Make rs34371500(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969518
GeneF8
is asnp
is mentioned by
dbSNPrs34371500
ebirs34371500
HLIrs34371500
Exacrs34371500
Varsomers34371500
Maprs34371500
PheGenIrs34371500
hapmaprs34371500
1000 genomesrs34371500
hgdprs34371500
ensemblrs34371500
gopubmedrs34371500
geneviewrs34371500
scholarrs34371500
googlers34371500
pharmgkbrs34371500
gwascentralrs34371500
openSNPrs34371500
23andMers34371500
23andMe allrs34371500
SNP Nexus

SNPshotrs34371500
SNPdbers34371500
MSV3drs34371500
GWAS Ctlgrs34371500
Max Magnitude0
OMIM306700
Desc
Variant0103
Relatedalso


ClinVar
Risk rs34371500(A,T;A,T)
Alt rs34371500(A,T;A,T)
Reference rs34371500(G;G)
Significance Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154197793C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010899.3,



[PMID 18320046OA-icon.png] Common variants within MECP2 confer risk of systemic lupus erythematosus.