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rs121918303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918303(A;C)
Make rs121918303(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position31777398
GeneRXFP2
is asnp
is mentioned by
dbSNPrs121918303
ebirs121918303
HLIrs121918303
Exacrs121918303
Varsomers121918303
Maprs121918303
PheGenIrs121918303
hapmaprs121918303
1000 genomesrs121918303
hgdprs121918303
ensemblrs121918303
gopubmedrs121918303
geneviewrs121918303
scholarrs121918303
googlers121918303
pharmgkbrs121918303
gwascentralrs121918303
openSNPrs121918303
23andMers121918303
23andMe allrs121918303
SNP Nexus

SNPshotrs121918303
SNPdbers121918303
MSV3drs121918303
GWAS Ctlgrs121918303
Merged fromRs28939382
GMAF0.001837
Max Magnitude0
OMIM606655
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918303(C,G;C,G)
Alt rs121918303(C,G;C,G)
Reference rs121918303(A;A)
Significance Pathogenic
Disease Cryptorchidism
Variation info
Gene RXFP2
CLNDBN Cryptorchidism, unilateral or bilateral
Reversed 0
HGVS NC_000013.10:g.32351535A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004376.3,