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rs1064796708

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome1
Position241497916
GeneFH
is asnp
is mentioned by
dbSNPrs1064796708
dbSNP (classic)rs1064796708
ClinGenrs1064796708
ebirs1064796708
HLIrs1064796708
Exacrs1064796708
Gnomadrs1064796708
Varsomers1064796708
LitVarrs1064796708
Maprs1064796708
PheGenIrs1064796708
Biobankrs1064796708
1000 genomesrs1064796708
hgdprs1064796708
ensemblrs1064796708
geneviewrs1064796708
scholarrs1064796708
googlers1064796708
pharmgkbrs1064796708
gwascentralrs1064796708
openSNPrs1064796708
23andMers1064796708
23andMe allrs1064796708
SNPshotrs1064796708
SNPdbers1064796708
MSV3drs1064796708
GWAS Ctlgrs1064796708
Max Magnitude0
ClinVar
Risk rs1064796708(G;G)
Alt rs1064796708(G;G)
Reference Rs1064796708(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.241661216A>C
CLNSRC
CLNACC RCV000485484.1,