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rs199469469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs199469469(-;-)
Make rs199469469(-;AAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position127426123
GenePROC
is asnp
is mentioned by
dbSNPrs199469469
ebirs199469469
HLIrs199469469
Exacrs199469469
Varsomers199469469
Maprs199469469
PheGenIrs199469469
hapmaprs199469469
1000 genomesrs199469469
hgdprs199469469
ensemblrs199469469
gopubmedrs199469469
geneviewrs199469469
scholarrs199469469
googlers199469469
pharmgkbrs199469469
gwascentralrs199469469
openSNPrs199469469
23andMers199469469
23andMe allrs199469469
SNP Nexus

SNPshotrs199469469
SNPdbers199469469
MSV3drs199469469
GWAS Ctlgrs199469469
Max Magnitude0
ClinVar
Risk rs199469469(;)
Alt rs199469469(;)
Reference rs199469469(AAG;AAG)
Significance Probable-Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein c deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128183699_128183701delAAG
CLNSRC
CLNACC