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rs387907086

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907086(A;A)
Make rs387907086(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position20431099
GeneSCARF2
is asnp
is mentioned by
dbSNPrs387907086
ebirs387907086
HLIrs387907086
Exacrs387907086
Varsomers387907086
Maprs387907086
PheGenIrs387907086
hapmaprs387907086
1000 genomesrs387907086
hgdprs387907086
ensemblrs387907086
gopubmedrs387907086
geneviewrs387907086
scholarrs387907086
googlers387907086
pharmgkbrs387907086
gwascentralrs387907086
openSNPrs387907086
23andMers387907086
23andMe allrs387907086
SNP Nexus

SNPshotrs387907086
SNPdbers387907086
MSV3drs387907086
GWAS Ctlgrs387907086
Max Magnitude0
ClinVar
Risk rs387907086(A;A)
Alt rs387907086(A;A)
Reference rs387907086(G;G)
Significance Pathogenic
Disease Marden Walker like syndrome
Variation info
Gene SCARF2
CLNDBN Marden Walker like syndrome
Reversed 1
HGVS NC_000022.10:g.20785386C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024040.3,