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rs121918122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918122(A;A)
Make rs121918122(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position186669945
GeneHRG
is asnp
is mentioned by
dbSNPrs121918122
ebirs121918122
HLIrs121918122
Exacrs121918122
Varsomers121918122
Maprs121918122
PheGenIrs121918122
hapmaprs121918122
1000 genomesrs121918122
hgdprs121918122
ensemblrs121918122
gopubmedrs121918122
geneviewrs121918122
scholarrs121918122
googlers121918122
pharmgkbrs121918122
gwascentralrs121918122
openSNPrs121918122
23andMers121918122
23andMe allrs121918122
SNP Nexus

SNPshotrs121918122
SNPdbers121918122
MSV3drs121918122
GWAS Ctlgrs121918122
Max Magnitude0
OMIM142640
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918122(A;A)
Alt rs121918122(A;A)
Reference rs121918122(G;G)
Significance Pathogenic
Disease Thrombophilia
Variation info
Gene HRG
CLNDBN Thrombophilia, histidine-rich glycoprotein-related
Reversed 0
HGVS NC_000003.11:g.186387734G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016049.25,