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rs1363364

From SNPedia

Orientationplus
Stabilizedplus
Make rs1363364(A;A)
Make rs1363364(A;T)
Make rs1363364(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position34817436
GenePEX11B
is asnp
is mentioned by
dbSNPrs1363364
ebirs1363364
HLIrs1363364
Exacrs1363364
Varsomers1363364
Maprs1363364
PheGenIrs1363364
hapmaprs1363364
1000 genomesrs1363364
hgdprs1363364
ensemblrs1363364
gopubmedrs1363364
geneviewrs1363364
scholarrs1363364
googlers1363364
pharmgkbrs1363364
gwascentralrs1363364
openSNPrs1363364
23andMers1363364
23andMe allrs1363364
SNP Nexus

SNPshotrs1363364
SNPdbers1363364
MSV3drs1363364
GWAS Ctlgrs1363364
GMAF0.4702
Max Magnitude
? (A;A) (A;T) (T;T) 28
OMIM270420
DescDIARRHEA 3, SECRETORY SODIUM, CONGENITAL; DIAR3
Variant
Relatedalso
[PMID 19185281OA-icon.png] Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.