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rs1064795320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position241497972
GeneFH
is asnp
is mentioned by
dbSNPrs1064795320
dbSNP (classic)rs1064795320
ClinGenrs1064795320
ebirs1064795320
HLIrs1064795320
Exacrs1064795320
Gnomadrs1064795320
Varsomers1064795320
LitVarrs1064795320
Maprs1064795320
PheGenIrs1064795320
Biobankrs1064795320
1000 genomesrs1064795320
hgdprs1064795320
ensemblrs1064795320
geneviewrs1064795320
scholarrs1064795320
googlers1064795320
pharmgkbrs1064795320
gwascentralrs1064795320
openSNPrs1064795320
23andMers1064795320
23andMe allrs1064795320
SNPshotrs1064795320
SNPdbers1064795320
MSV3drs1064795320
GWAS Ctlgrs1064795320
Max Magnitude0
ClinVar
Risk rs1064795320(-;-)
Alt rs1064795320(-;-)
Reference Rs1064795320(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661272delT
CLNSRC
CLNACC RCV000486287.1,