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rs757583846

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757583846(C;T)
Make rs757583846(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position127421381
GenePROC
is asnp
is mentioned by
dbSNPrs757583846
ebirs757583846
HLIrs757583846
Exacrs757583846
Varsomers757583846
Maprs757583846
PheGenIrs757583846
hapmaprs757583846
1000 genomesrs757583846
hgdprs757583846
ensemblrs757583846
gopubmedrs757583846
geneviewrs757583846
scholarrs757583846
googlers757583846
pharmgkbrs757583846
gwascentralrs757583846
openSNPrs757583846
23andMers757583846
23andMe allrs757583846
SNP Nexus

SNPshotrs757583846
SNPdbers757583846
MSV3drs757583846
GWAS Ctlgrs757583846
Max Magnitude0
ClinVar
Risk rs757583846(T;T)
Alt rs757583846(T;T)
Reference rs757583846(C;C)
Significance Pathogenic
Disease Thrombophilia
Variation info
Gene PROC
CLNDBN Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.128178957C>T
CLNSRC
CLNACC RCV000168170.2,