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rs386834226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386834226(-;-)
Make rs386834226(-;A)
Make rs386834226(A;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position169541903
GeneF5
is asnp
is mentioned by
dbSNPrs386834226
ebirs386834226
HLIrs386834226
Exacrs386834226
Varsomers386834226
Maprs386834226
PheGenIrs386834226
hapmaprs386834226
1000 genomesrs386834226
hgdprs386834226
ensemblrs386834226
gopubmedrs386834226
geneviewrs386834226
scholarrs386834226
googlers386834226
pharmgkbrs386834226
gwascentralrs386834226
openSNPrs386834226
23andMers386834226
23andMe allrs386834226
SNP Nexus

SNPshotrs386834226
SNPdbers386834226
MSV3drs386834226
GWAS Ctlgrs386834226
Max Magnitude0
ClinVar
Risk rs386834226(A;A)
Alt rs386834226(A;A)
Reference rs386834226(;)
Significance Pathogenic
Disease not provided
Variation info
Gene F5
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.169511142dupT
CLNSRC ClinVar
CLNACC RCV000049569.1,