Rs118204455

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118204455(A;G)
Make rs118204455(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position177406019
GeneF12
is asnp
is mentioned by
dbSNPrs118204455
Exacrs118204455
PheGenIrs118204455
nextbiors118204455
hapmaprs118204455
1000 genomesrs118204455
hgdprs118204455
ensemblrs118204455
gopubmedrs118204455
geneviewrs118204455
scholarrs118204455
googlers118204455
pharmgkbrs118204455
gwascentralrs118204455
openSNPrs118204455
23andMers118204455
23andMe allrs118204455
SNP Nexus

SNPshotrs118204455
SNPdbers118204455
MSV3drs118204455
Max Magnitude0
OMIM610619
Desc
Variant0005
Relatedalso
ClinVar
Risk rs118204455(G;G)
Alt rs118204455(G;G)
Reference rs118204455(A;A)
Significance Pathogenic
Disease FACTOR XII (TENRI)
Variation info
Gene F12
CLNDBN FACTOR XII (TENRI)
Reversed 1
HGVS NC_000005.9:g.176833020T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001227.2,