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rs377074720

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377074720(A;A)
Make rs377074720(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position187236295
GeneMASP1
is asnp
is mentioned by
dbSNPrs377074720
ebirs377074720
HLIrs377074720
Exacrs377074720
Varsomers377074720
Maprs377074720
PheGenIrs377074720
hapmaprs377074720
1000 genomesrs377074720
hgdprs377074720
ensemblrs377074720
gopubmedrs377074720
geneviewrs377074720
scholarrs377074720
googlers377074720
pharmgkbrs377074720
gwascentralrs377074720
openSNPrs377074720
23andMers377074720
23andMe allrs377074720
SNP Nexus

SNPshotrs377074720
SNPdbers377074720
MSV3drs377074720
GWAS Ctlgrs377074720
Max Magnitude0
ClinVar
Risk rs377074720(A;A)
Alt rs377074720(A;A)
Reference rs377074720(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MASP1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.186954083G>A
CLNSRC
CLNACC RCV000171372.1,