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rs796051875

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051875(A;A)
Make rs796051875(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position208909
GeneFAM20C
is asnp
is mentioned by
dbSNPrs796051875
ebirs796051875
HLIrs796051875
Exacrs796051875
Varsomers796051875
Maprs796051875
PheGenIrs796051875
hapmaprs796051875
1000 genomesrs796051875
hgdprs796051875
ensemblrs796051875
gopubmedrs796051875
geneviewrs796051875
scholarrs796051875
googlers796051875
pharmgkbrs796051875
gwascentralrs796051875
openSNPrs796051875
23andMers796051875
23andMe allrs796051875
SNP Nexus

SNPshotrs796051875
SNPdbers796051875
MSV3drs796051875
GWAS Ctlgrs796051875
Max Magnitude0
ClinVar
Risk rs796051875(A;A)
Alt rs796051875(A;A)
Reference rs796051875(G;G)
Significance Pathogenic
Disease Raine syndrome
Variation info
Gene FAM20C
CLNDBN Raine syndrome
Reversed 0
HGVS NC_000007.13:g.208909G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023862.4,