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rs1064795155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position215428331
GeneFN1
is asnp
is mentioned by
dbSNPrs1064795155
dbSNP (old)rs1064795155
ClinGenrs1064795155
ebirs1064795155
HLIrs1064795155
Exacrs1064795155
Gnomadrs1064795155
Varsomers1064795155
LitVarrs1064795155
Maprs1064795155
PheGenIrs1064795155
Biobankrs1064795155
1000 genomesrs1064795155
hgdprs1064795155
ensemblrs1064795155
gopubmedrs1064795155
geneviewrs1064795155
scholarrs1064795155
googlers1064795155
pharmgkbrs1064795155
gwascentralrs1064795155
openSNPrs1064795155
23andMers1064795155
23andMe allrs1064795155
SNPshotrs1064795155
SNPdbers1064795155
MSV3drs1064795155
GWAS Ctlgrs1064795155
Max Magnitude0
ClinVar
Risk rs1064795155(G;G)
Alt rs1064795155(G;G)
Reference Rs1064795155(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FN1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.216293054G>C
CLNSRC
CLNACC RCV000480973.1,