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rs786205883

From SNPedia

Orientationminus
Geno Mag Summary
(CTGGGGCGCGCGCTGCG;CTGGGGCGCGCGCTGCG) 0 common in clinvar
Make rs786205883(-;-)
Make rs786205883(-;CTGGGGCGCGCGCTGCG)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position20431415
GeneSCARF2
is asnp
is mentioned by
dbSNPrs786205883
ebirs786205883
HLIrs786205883
Exacrs786205883
Varsomers786205883
Maprs786205883
PheGenIrs786205883
hapmaprs786205883
1000 genomesrs786205883
hgdprs786205883
ensemblrs786205883
gopubmedrs786205883
geneviewrs786205883
scholarrs786205883
googlers786205883
pharmgkbrs786205883
gwascentralrs786205883
openSNPrs786205883
23andMers786205883
23andMe allrs786205883
SNP Nexus

SNPshotrs786205883
SNPdbers786205883
MSV3drs786205883
GWAS Ctlgrs786205883
Max Magnitude0
ClinVar
Risk rs786205883(;)
Alt rs786205883(;)
Reference rs786205883(CTGGGGCGCGCGCTGCG;CTGGGGCGCGCGCTGCG)
Significance Pathogenic
Disease Marden Walker like syndrome
Variation info
Gene SCARF2
CLNDBN Marden Walker like syndrome
Reversed 1
HGVS NC_000022.10:g.20785702_20785718del17
CLNSRC OMIM Allelic Variant
CLNACC RCV000170462.3,