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rs886039431

From SNPedia

Merged intors113993990
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039431(-;-)
Make rs886039431(-;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position66995298
GeneSBDS, TYW1
is asnp
is mentioned by
dbSNPrs886039431
dbSNP (classic)rs886039431
ClinGenrs886039431
ebirs886039431
HLIrs886039431
Exacrs886039431
Gnomadrs886039431
Varsomers886039431
LitVarrs886039431
Maprs886039431
PheGenIrs886039431
Biobankrs886039431
1000 genomesrs886039431
hgdprs886039431
ensemblrs886039431
geneviewrs886039431
scholarrs886039431
googlers886039431
pharmgkbrs886039431
gwascentralrs886039431
openSNPrs886039431
23andMers886039431
23andMe allrs886039431
SNPshotrs886039431
SNPdbers886039431
MSV3drs886039431
GWAS Ctlgrs886039431
StatusMerged into rs113993990
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs886039431(G;G)
Significance Pathogenic
Disease Shwachman syndrome not provided
Variation info
Gene SBDS TYW1
CLNDBN Shwachman syndrome not provided
Reversed 1
HGVS NC_000007.13:g.66460285delC
CLNSRC
CLNACC RCV000020725.1, RCV000255360.1,