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rs1064793125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome1
Position241508775
GeneFH
is asnp
is mentioned by
dbSNPrs1064793125
dbSNP (old)rs1064793125
ClinGenrs1064793125
ebirs1064793125
HLIrs1064793125
Exacrs1064793125
Gnomadrs1064793125
Varsomers1064793125
LitVarrs1064793125
Maprs1064793125
PheGenIrs1064793125
Biobankrs1064793125
1000 genomesrs1064793125
hgdprs1064793125
ensemblrs1064793125
gopubmedrs1064793125
geneviewrs1064793125
scholarrs1064793125
googlers1064793125
pharmgkbrs1064793125
gwascentralrs1064793125
openSNPrs1064793125
23andMers1064793125
23andMe allrs1064793125
SNPshotrs1064793125
SNPdbers1064793125
MSV3drs1064793125
GWAS Ctlgrs1064793125
Max Magnitude0
ClinVar
Risk rs1064793125(T;T)
Alt rs1064793125(T;T)
Reference Rs1064793125(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241672075T>A
CLNSRC
CLNACC RCV000478475.1,