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rs6020

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6020(A;A)
Make rs6020(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169549874
GeneF5
is asnp
is mentioned by
dbSNPrs6020
dbSNP (classic)rs6020
ClinGenrs6020
ebirs6020
HLIrs6020
Exacrs6020
Gnomadrs6020
Varsomers6020
LitVarrs6020
Maprs6020
PheGenIrs6020
Biobankrs6020
1000 genomesrs6020
hgdprs6020
ensemblrs6020
geneviewrs6020
scholarrs6020
googlers6020
pharmgkbrs6020
gwascentralrs6020
openSNPrs6020
23andMers6020
SNPshotrs6020
SNPdbers6020
MSV3drs6020
GWAS Ctlgrs6020
GMAF0.2649
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23954867] The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes


[PMID 18974781OA-icon.png] Cataloging coding sequence variations in human genome databases.


[PMID 25119470OA-icon.png] Single Nucleotide Polymorphisms Other than Factor V Leiden Are Associated with Coagulopathy and Osteonecrosis of the Femoral Head in Chinese Patients


ClinVar
Risk rs6020(A;A)
Alt rs6020(A;A)
Reference Rs6020(G;G)
Significance Probable-non-pathogenic
Disease Thrombophilia due to activated protein C resistance
Variation info
Gene F5
CLNDBN Thrombophilia due to activated protein C resistance
Reversed 1
HGVS NC_000001.10:g.169519112C>T
CLNSRC
CLNACC RCV000333894.1,