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

rs796051849

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051849(G;G)
Make rs796051849(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position255939
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051849
ebirs796051849
HLIrs796051849
Exacrs796051849
Varsomers796051849
Maprs796051849
PheGenIrs796051849
hapmaprs796051849
1000 genomesrs796051849
hgdprs796051849
ensemblrs796051849
gopubmedrs796051849
geneviewrs796051849
scholarrs796051849
googlers796051849
pharmgkbrs796051849
gwascentralrs796051849
openSNPrs796051849
23andMers796051849
23andMe allrs796051849
SNP Nexus

SNPshotrs796051849
SNPdbers796051849
MSV3drs796051849
GWAS Ctlgrs796051849
Max Magnitude0
ClinVar
Risk rs796051849(G;G)
Alt rs796051849(G;G)
Reference rs796051849(T;T)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.295905T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001079.3,