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rs796051874

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051874(A;A)
Make rs796051874(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position195685
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051874
ebirs796051874
HLIrs796051874
Exacrs796051874
Varsomers796051874
Maprs796051874
PheGenIrs796051874
hapmaprs796051874
1000 genomesrs796051874
hgdprs796051874
ensemblrs796051874
gopubmedrs796051874
geneviewrs796051874
scholarrs796051874
googlers796051874
pharmgkbrs796051874
gwascentralrs796051874
openSNPrs796051874
23andMers796051874
23andMe allrs796051874
SNP Nexus

SNPshotrs796051874
SNPdbers796051874
MSV3drs796051874
GWAS Ctlgrs796051874
Max Magnitude0
ClinVar
Risk rs796051874(A;A)
Alt rs796051874(A;A)
Reference rs796051874(T;T)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.195685T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023861.3,