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rs886054846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Chromosome2
Position127426126
GeneLOC105373608, PROC
is asnp
is mentioned by
dbSNPrs886054846
dbSNP (classic)rs886054846
ClinGenrs886054846
ebirs886054846
HLIrs886054846
Exacrs886054846
Gnomadrs886054846
Varsomers886054846
LitVarrs886054846
Maprs886054846
PheGenIrs886054846
Biobankrs886054846
1000 genomesrs886054846
hgdprs886054846
ensemblrs886054846
geneviewrs886054846
scholarrs886054846
googlers886054846
pharmgkbrs886054846
gwascentralrs886054846
openSNPrs886054846
23andMers886054846
SNPshotrs886054846
SNPdbers886054846
MSV3drs886054846
GWAS Ctlgrs886054846
Max Magnitude0
ClinVar
Risk rs886054846(-;-)
Alt rs886054846(-;-)
Reference Rs886054846(AGA;AGA)
Significance Other
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128183702_128183704delAAG
CLNSRC Illumina
CLNACC RCV000288890.1,