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rs797044906

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044906(G;T)
Make rs797044906(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position215404591
GeneFN1
is asnp
is mentioned by
dbSNPrs797044906
ebirs797044906
HLIrs797044906
Exacrs797044906
Varsomers797044906
Maprs797044906
PheGenIrs797044906
hapmaprs797044906
1000 genomesrs797044906
hgdprs797044906
ensemblrs797044906
gopubmedrs797044906
geneviewrs797044906
scholarrs797044906
googlers797044906
pharmgkbrs797044906
gwascentralrs797044906
openSNPrs797044906
23andMers797044906
23andMe allrs797044906
SNP Nexus

SNPshotrs797044906
SNPdbers797044906
MSV3drs797044906
GWAS Ctlgrs797044906
Max Magnitude0
ClinVar
Risk rs797044906(T;T)
Alt rs797044906(T;T)
Reference rs797044906(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FN1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.216269314C>A
CLNSRC
CLNACC RCV000190733.1,