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rs199469508

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199469508(C;C)
Make rs199469508(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173917217
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs199469508
ebirs199469508
HLIrs199469508
Exacrs199469508
Varsomers199469508
Maprs199469508
PheGenIrs199469508
hapmaprs199469508
1000 genomesrs199469508
hgdprs199469508
ensemblrs199469508
gopubmedrs199469508
geneviewrs199469508
scholarrs199469508
googlers199469508
pharmgkbrs199469508
gwascentralrs199469508
openSNPrs199469508
23andMers199469508
23andMe allrs199469508
SNP Nexus

SNPshotrs199469508
SNPdbers199469508
MSV3drs199469508
GWAS Ctlgrs199469508
Max Magnitude0
ClinVar
Risk rs199469508(C;C)
Alt rs199469508(C;C)
Reference rs199469508(T;T)
Significance Untested
Disease
Variation info
Gene SERPINC1
CLNDBN OMIM
Reversed 1
HGVS NC_000001.10:g.173886355A>G
CLNSRC
CLNACC