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

rs796051855

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051855(A;A)
Make rs796051855(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position258645
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051855
ebirs796051855
HLIrs796051855
Exacrs796051855
Varsomers796051855
Maprs796051855
PheGenIrs796051855
hapmaprs796051855
1000 genomesrs796051855
hgdprs796051855
ensemblrs796051855
gopubmedrs796051855
geneviewrs796051855
scholarrs796051855
googlers796051855
pharmgkbrs796051855
gwascentralrs796051855
openSNPrs796051855
23andMers796051855
23andMe allrs796051855
SNP Nexus

SNPshotrs796051855
SNPdbers796051855
MSV3drs796051855
GWAS Ctlgrs796051855
Max Magnitude0
ClinVar
Risk rs796051855(A;A)
Alt rs796051855(A;A)
Reference rs796051855(G;G)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.298611G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001085.4,