Have questions? Visit https://www.reddit.com/r/SNPedia

rs796051851

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051851(C;G)
Make rs796051851(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position248312
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051851
ebirs796051851
HLIrs796051851
Exacrs796051851
Varsomers796051851
Maprs796051851
PheGenIrs796051851
hapmaprs796051851
1000 genomesrs796051851
hgdprs796051851
ensemblrs796051851
gopubmedrs796051851
geneviewrs796051851
scholarrs796051851
googlers796051851
pharmgkbrs796051851
gwascentralrs796051851
openSNPrs796051851
23andMers796051851
23andMe allrs796051851
SNP Nexus

SNPshotrs796051851
SNPdbers796051851
MSV3drs796051851
GWAS Ctlgrs796051851
Max Magnitude0
ClinVar
Risk rs796051851(G;G)
Alt rs796051851(G;G)
Reference rs796051851(C;C)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.288278C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001081.3,