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rs796052138

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs796052138(-;-)
Make rs796052138(-;AGA)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position196679674
GeneCFH
is asnp
is mentioned by
dbSNPrs796052138
ebirs796052138
HLIrs796052138
Exacrs796052138
Varsomers796052138
Maprs796052138
PheGenIrs796052138
hapmaprs796052138
1000 genomesrs796052138
hgdprs796052138
ensemblrs796052138
gopubmedrs796052138
geneviewrs796052138
scholarrs796052138
googlers796052138
pharmgkbrs796052138
gwascentralrs796052138
openSNPrs796052138
23andMers796052138
23andMe allrs796052138
SNP Nexus

SNPshotrs796052138
SNPdbers796052138
MSV3drs796052138
GWAS Ctlgrs796052138
Max Magnitude0
ClinVar
Risk rs796052138(;)
Alt rs796052138(;)
Reference rs796052138(AGA;AGA)
Significance Pathogenic
Disease Factor H deficiency
Variation info
Gene CFH
CLNDBN Factor H deficiency
Reversed 0
HGVS NC_000001.10:g.196648804_196648806delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000018022.28,