Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position241513715
GeneFH
is asnp
is mentioned by
dbSNPrs1064793741
dbSNP (old)rs1064793741
ClinGenrs1064793741
ebirs1064793741
HLIrs1064793741
Exacrs1064793741
Gnomadrs1064793741
Varsomers1064793741
LitVarrs1064793741
Maprs1064793741
PheGenIrs1064793741
Biobankrs1064793741
1000 genomesrs1064793741
hgdprs1064793741
ensemblrs1064793741
gopubmedrs1064793741
geneviewrs1064793741
scholarrs1064793741
googlers1064793741
pharmgkbrs1064793741
gwascentralrs1064793741
openSNPrs1064793741
23andMers1064793741
23andMe allrs1064793741
SNPshotrs1064793741
SNPdbers1064793741
MSV3drs1064793741
GWAS Ctlgrs1064793741
Max Magnitude0
ClinVar
Risk rs1064793741(G;G)
Alt rs1064793741(G;G)
Reference Rs1064793741(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241677015T>C
CLNSRC
CLNACC RCV000487137.1,