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rs796051853

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051853(A;G)
Make rs796051853(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position257003
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051853
ebirs796051853
HLIrs796051853
Exacrs796051853
Varsomers796051853
Maprs796051853
PheGenIrs796051853
hapmaprs796051853
1000 genomesrs796051853
hgdprs796051853
ensemblrs796051853
gopubmedrs796051853
geneviewrs796051853
scholarrs796051853
googlers796051853
pharmgkbrs796051853
gwascentralrs796051853
openSNPrs796051853
23andMers796051853
23andMe allrs796051853
SNP Nexus

SNPshotrs796051853
SNPdbers796051853
MSV3drs796051853
GWAS Ctlgrs796051853
Max Magnitude0
ClinVar
Risk rs796051853(G;G)
Alt rs796051853(G;G)
Reference rs796051853(A;A)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.296969A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001083.4,