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rs796051854

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051854(C;C)
Make rs796051854(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position246512
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051854
ebirs796051854
HLIrs796051854
Exacrs796051854
Varsomers796051854
Maprs796051854
PheGenIrs796051854
hapmaprs796051854
1000 genomesrs796051854
hgdprs796051854
ensemblrs796051854
gopubmedrs796051854
geneviewrs796051854
scholarrs796051854
googlers796051854
pharmgkbrs796051854
gwascentralrs796051854
openSNPrs796051854
23andMers796051854
23andMe allrs796051854
SNP Nexus

SNPshotrs796051854
SNPdbers796051854
MSV3drs796051854
GWAS Ctlgrs796051854
Max Magnitude0
ClinVar
Risk rs796051854(C;C)
Alt rs796051854(C;C)
Reference rs796051854(G;G)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.286478G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001084.4,