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rs786205233

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205233(A;G)
Make rs786205233(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132934305
GeneAFF4
is asnp
is mentioned by
dbSNPrs786205233
ebirs786205233
HLIrs786205233
Exacrs786205233
Varsomers786205233
Maprs786205233
PheGenIrs786205233
hapmaprs786205233
1000 genomesrs786205233
hgdprs786205233
ensemblrs786205233
gopubmedrs786205233
geneviewrs786205233
scholarrs786205233
googlers786205233
pharmgkbrs786205233
gwascentralrs786205233
openSNPrs786205233
23andMers786205233
23andMe allrs786205233
SNP Nexus

SNPshotrs786205233
SNPdbers786205233
MSV3drs786205233
GWAS Ctlgrs786205233
Max Magnitude0
ClinVar
Risk rs786205233(G;G)
Alt rs786205233(G;G)
Reference rs786205233(A;A)
Significance Pathogenic
Disease Chops syndrome
Variation info
Gene AFF4
CLNDBN Chops syndrome
Reversed 1
HGVS NC_000005.9:g.132269997T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170515.3,