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rs386834227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386834227(A;A)
Make rs386834227(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169529635
GeneF5
is asnp
is mentioned by
dbSNPrs386834227
ebirs386834227
HLIrs386834227
Exacrs386834227
Varsomers386834227
Maprs386834227
PheGenIrs386834227
hapmaprs386834227
1000 genomesrs386834227
hgdprs386834227
ensemblrs386834227
gopubmedrs386834227
geneviewrs386834227
scholarrs386834227
googlers386834227
pharmgkbrs386834227
gwascentralrs386834227
openSNPrs386834227
23andMers386834227
23andMe allrs386834227
SNP Nexus

SNPshotrs386834227
SNPdbers386834227
MSV3drs386834227
GWAS Ctlgrs386834227
Max Magnitude0
ClinVar
Risk rs386834227(A;A)
Alt rs386834227(A;A)
Reference rs386834227(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene F5
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.169498873C>T
CLNSRC ClinVar
CLNACC RCV000049570.1,