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rs786205679

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205679(C;G)
Make rs786205679(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132934304
GeneAFF4
is asnp
is mentioned by
dbSNPrs786205679
ebirs786205679
HLIrs786205679
Exacrs786205679
Varsomers786205679
Maprs786205679
PheGenIrs786205679
hapmaprs786205679
1000 genomesrs786205679
hgdprs786205679
ensemblrs786205679
gopubmedrs786205679
geneviewrs786205679
scholarrs786205679
googlers786205679
pharmgkbrs786205679
gwascentralrs786205679
openSNPrs786205679
23andMers786205679
23andMe allrs786205679
SNP Nexus

SNPshotrs786205679
SNPdbers786205679
MSV3drs786205679
GWAS Ctlgrs786205679
Max Magnitude0
ClinVar
Risk rs786205679(G;G)
Alt rs786205679(G;G)
Reference rs786205679(C;C)
Significance Pathogenic
Disease Chops syndrome
Variation info
Gene AFF4
CLNDBN Chops syndrome
Reversed 1
HGVS NC_000005.9:g.132269996G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170516.3,