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rs2227598

From SNPedia

Orientationminus
Stabilizedminus
Make rs2227598(C;C)
Make rs2227598(C;T)
Make rs2227598(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position173915033
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs2227598
ebirs2227598
HLIrs2227598
Exacrs2227598
Varsomers2227598
Maprs2227598
PheGenIrs2227598
hapmaprs2227598
1000 genomesrs2227598
hgdprs2227598
ensemblrs2227598
gopubmedrs2227598
geneviewrs2227598
scholarrs2227598
googlers2227598
pharmgkbrs2227598
gwascentralrs2227598
openSNPrs2227598
23andMers2227598
23andMe allrs2227598
SNP Nexus

SNPshotrs2227598
SNPdbers2227598
MSV3drs2227598
GWAS Ctlgrs2227598
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 25811371OA-icon.png] Antithrombin III Deficiency in Indian Patients with Deep Vein Thrombosis: Identification of First India Based AT Variants Including a Novel Point Mutation (T280A) that Leads to Aggregation