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rs375801610

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375801610(A;A)
Make rs375801610(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position50262168
GeneCFAP53, LOC105376869
is asnp
is mentioned by
dbSNPrs375801610
ebirs375801610
HLIrs375801610
Exacrs375801610
Varsomers375801610
Maprs375801610
PheGenIrs375801610
hapmaprs375801610
1000 genomesrs375801610
hgdprs375801610
ensemblrs375801610
gopubmedrs375801610
geneviewrs375801610
scholarrs375801610
googlers375801610
pharmgkbrs375801610
gwascentralrs375801610
openSNPrs375801610
23andMers375801610
23andMe allrs375801610
SNP Nexus

SNPshotrs375801610
SNPdbers375801610
MSV3drs375801610
GWAS Ctlgrs375801610
Max Magnitude0
ClinVar
Risk rs375801610(A;A)
Alt rs375801610(A;A)
Reference rs375801610(G;G)
Significance Pathogenic
Disease Heterotaxy
Variation info
Gene CFAP53
CLNDBN Heterotaxy, visceral, 6, autosomal
Reversed 0
HGVS NC_000018.9:g.47788538G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190555.2,