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rs755436052

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755436052(A;A)
Make rs755436052(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504102
GeneFH
is asnp
is mentioned by
dbSNPrs755436052
ebirs755436052
HLIrs755436052
Exacrs755436052
Varsomers755436052
Maprs755436052
PheGenIrs755436052
hapmaprs755436052
1000 genomesrs755436052
hgdprs755436052
ensemblrs755436052
gopubmedrs755436052
geneviewrs755436052
scholarrs755436052
googlers755436052
pharmgkbrs755436052
gwascentralrs755436052
openSNPrs755436052
23andMers755436052
23andMe allrs755436052
SNP Nexus

SNPshotrs755436052
SNPdbers755436052
MSV3drs755436052
GWAS Ctlgrs755436052
Max Magnitude0
ClinVar
Risk rs755436052(A;A)
Alt rs755436052(A;A)
Reference rs755436052(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FH
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.241667402G>A
CLNSRC
CLNACC RCV000198662.2,