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rs200635937

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs200635937(A;T)
Make rs200635937(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position168104855
GeneGPR161
is asnp
is mentioned by
dbSNPrs200635937
ebirs200635937
HLIrs200635937
Exacrs200635937
Varsomers200635937
Maprs200635937
PheGenIrs200635937
hapmaprs200635937
1000 genomesrs200635937
hgdprs200635937
ensemblrs200635937
gopubmedrs200635937
geneviewrs200635937
scholarrs200635937
googlers200635937
pharmgkbrs200635937
gwascentralrs200635937
openSNPrs200635937
23andMers200635937
23andMe allrs200635937
SNP Nexus

SNPshotrs200635937
SNPdbers200635937
MSV3drs200635937
GWAS Ctlgrs200635937
Max Magnitude0
ClinVar
Risk rs200635937(T;T)
Alt rs200635937(T;T)
Reference rs200635937(A;A)
Significance Probable-Pathogenic
Disease not provided Pituitary stalk interruption syndrome
Variation info
Gene GPR161
CLNDBN not provided Pituitary stalk interruption syndrome
Reversed 0
HGVS NC_000001.10:g.168074093A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157613.3, RCV000202520.1,