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rs6063

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 2
(A;G) None
(G;G) 0 common
ReferenceGRCh38 38.1/142
Chromosome4
Position154609725
GeneFGG
is asnp
is mentioned by
dbSNPrs6063
ebirs6063
HLIrs6063
Exacrs6063
Varsomers6063
Maprs6063
PheGenIrs6063
hapmaprs6063
1000 genomesrs6063
hgdprs6063
ensemblrs6063
gopubmedrs6063
geneviewrs6063
scholarrs6063
googlers6063
pharmgkbrs6063
gwascentralrs6063
openSNPrs6063
23andMers6063
23andMe allrs6063
SNP Nexus

SNPshotrs6063
SNPdbers6063
MSV3drs6063
GWAS Ctlgrs6063
GMAF0.006428
Max Magnitude2
? (A;A) (A;G) (G;G) 28
OMIM134850
DescFIBRINOGEN MILANO XII, DIGENIC
Variant0018
Relatedalso

This is the first snp to experiment with the watson alignment.


ClinVar
Risk rs6063(A;A)
Alt rs6063(A;A)
Reference rs6063(G;G)
Significance Pathogenic
Disease Fibrinogen Milano XII
Variation info
Gene FGG
CLNDBN Fibrinogen Milano XII, digenic
Reversed 1
HGVS NC_000004.11:g.155530877C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017800.4,