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rs752941297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752941297(C;T)
Make rs752941297(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position148097875
GeneSPINK5
is asnp
is mentioned by
dbSNPrs752941297
dbSNP (classic)rs752941297
ClinGenrs752941297
ebirs752941297
HLIrs752941297
Exacrs752941297
Gnomadrs752941297
Varsomers752941297
LitVarrs752941297
Maprs752941297
PheGenIrs752941297
Biobankrs752941297
1000 genomesrs752941297
hgdprs752941297
ensemblrs752941297
geneviewrs752941297
scholarrs752941297
googlers752941297
pharmgkbrs752941297
gwascentralrs752941297
openSNPrs752941297
23andMers752941297
SNPshotrs752941297
SNPdbers752941297
MSV3drs752941297
GWAS Ctlgrs752941297
Max Magnitude0
ClinVar
Risk rs752941297(T;T)
Alt rs752941297(T;T)
Reference Rs752941297(C;C)
Significance Probable-Pathogenic
Disease Erythroderma Increased IgE level
Variation info
Gene SPINK5
CLNDBN Erythroderma Increased IgE level
Reversed 0
HGVS NC_000005.9:g.147477438C>T
CLNSRC
CLNACC RCV000415446.1,