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rs1057518067

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518067(C;C)
Make rs1057518067(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position148125722
GeneSPINK5
is asnp
is mentioned by
dbSNPrs1057518067
dbSNP (old)rs1057518067
ClinGenrs1057518067
ebirs1057518067
HLIrs1057518067
Exacrs1057518067
Gnomadrs1057518067
Varsomers1057518067
Maprs1057518067
PheGenIrs1057518067
Biobankrs1057518067
1000 genomesrs1057518067
hgdprs1057518067
ensemblrs1057518067
gopubmedrs1057518067
geneviewrs1057518067
scholarrs1057518067
googlers1057518067
pharmgkbrs1057518067
gwascentralrs1057518067
openSNPrs1057518067
23andMers1057518067
23andMe allrs1057518067
SNPshotrs1057518067
SNPdbers1057518067
MSV3drs1057518067
GWAS Ctlgrs1057518067
Max Magnitude0
ClinVar
Risk rs1057518067(C;C)
Alt rs1057518067(C;C)
Reference Rs1057518067(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPINK5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.147505285G>C
CLNSRC
CLNACC RCV000413920.1,