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rs1057518161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518161(C;C)
Make rs1057518161(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position148095907
GeneSPINK5
is asnp
is mentioned by
dbSNPrs1057518161
dbSNP (old)rs1057518161
ClinGenrs1057518161
ebirs1057518161
HLIrs1057518161
Exacrs1057518161
Gnomadrs1057518161
Varsomers1057518161
Maprs1057518161
PheGenIrs1057518161
Biobankrs1057518161
1000 genomesrs1057518161
hgdprs1057518161
ensemblrs1057518161
gopubmedrs1057518161
geneviewrs1057518161
scholarrs1057518161
googlers1057518161
pharmgkbrs1057518161
gwascentralrs1057518161
openSNPrs1057518161
23andMers1057518161
23andMe allrs1057518161
SNPshotrs1057518161
SNPdbers1057518161
MSV3drs1057518161
GWAS Ctlgrs1057518161
Max Magnitude0
ClinVar
Risk rs1057518161(C;C)
Alt rs1057518161(C;C)
Reference Rs1057518161(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SPINK5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.147475470T>C
CLNSRC
CLNACC RCV000413636.1,