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rs886039547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039547(C;T)
Make rs886039547(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position148070377
GeneSPINK5
is asnp
is mentioned by
dbSNPrs886039547
dbSNP (classic)rs886039547
ClinGenrs886039547
ebirs886039547
HLIrs886039547
Exacrs886039547
Gnomadrs886039547
Varsomers886039547
LitVarrs886039547
Maprs886039547
PheGenIrs886039547
Biobankrs886039547
1000 genomesrs886039547
hgdprs886039547
ensemblrs886039547
geneviewrs886039547
scholarrs886039547
googlers886039547
pharmgkbrs886039547
gwascentralrs886039547
openSNPrs886039547
23andMers886039547
SNPshotrs886039547
SNPdbers886039547
MSV3drs886039547
GWAS Ctlgrs886039547
Max Magnitude0
ClinVar
Risk rs886039547(T;T)
Alt rs886039547(T;T)
Reference Rs886039547(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SPINK5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.147449940C>T
CLNSRC
CLNACC RCV000255706.1,