Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064793126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position241508635
GeneFH
is asnp
is mentioned by
dbSNPrs1064793126
dbSNP (old)rs1064793126
ClinGenrs1064793126
ebirs1064793126
HLIrs1064793126
Exacrs1064793126
Gnomadrs1064793126
Varsomers1064793126
Maprs1064793126
PheGenIrs1064793126
Biobankrs1064793126
1000 genomesrs1064793126
hgdprs1064793126
ensemblrs1064793126
gopubmedrs1064793126
geneviewrs1064793126
scholarrs1064793126
googlers1064793126
pharmgkbrs1064793126
gwascentralrs1064793126
openSNPrs1064793126
23andMers1064793126
23andMe allrs1064793126
SNPshotrs1064793126
SNPdbers1064793126
MSV3drs1064793126
GWAS Ctlgrs1064793126
Max Magnitude0
ClinVar
Risk rs1064793126(G;G)
Alt rs1064793126(G;G)
Reference Rs1064793126(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241671935T>C
CLNSRC
CLNACC RCV000482578.1,