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rs796051852

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051852(A;A)
Make rs796051852(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position255912
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051852
ebirs796051852
HLIrs796051852
Exacrs796051852
Varsomers796051852
Maprs796051852
PheGenIrs796051852
hapmaprs796051852
1000 genomesrs796051852
hgdprs796051852
ensemblrs796051852
gopubmedrs796051852
geneviewrs796051852
scholarrs796051852
googlers796051852
pharmgkbrs796051852
gwascentralrs796051852
openSNPrs796051852
23andMers796051852
23andMe allrs796051852
SNP Nexus

SNPshotrs796051852
SNPdbers796051852
MSV3drs796051852
GWAS Ctlgrs796051852
Max Magnitude0
ClinVar
Risk rs796051852(A;A)
Alt rs796051852(A;A)
Reference rs796051852(G;G)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.295878G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001082.4,