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rs386834228

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386834228(A;A)
Make rs386834228(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169525949
GeneF5
is asnp
is mentioned by
dbSNPrs386834228
ebirs386834228
HLIrs386834228
Exacrs386834228
Varsomers386834228
Maprs386834228
PheGenIrs386834228
hapmaprs386834228
1000 genomesrs386834228
hgdprs386834228
ensemblrs386834228
gopubmedrs386834228
geneviewrs386834228
scholarrs386834228
googlers386834228
pharmgkbrs386834228
gwascentralrs386834228
openSNPrs386834228
23andMers386834228
23andMe allrs386834228
SNP Nexus

SNPshotrs386834228
SNPdbers386834228
MSV3drs386834228
GWAS Ctlgrs386834228
Max Magnitude0
ClinVar
Risk rs386834228(A;A)
Alt rs386834228(A;A)
Reference rs386834228(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene F5
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.169495187C>T
CLNSRC ClinVar
CLNACC RCV000049571.1,