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rs200834568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200834568(A;A)
Make rs200834568(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position105798763
is asnp
is mentioned by
dbSNPrs200834568
ebirs200834568
HLIrs200834568
Exacrs200834568
Varsomers200834568
Maprs200834568
PheGenIrs200834568
hapmaprs200834568
1000 genomesrs200834568
hgdprs200834568
ensemblrs200834568
gopubmedrs200834568
geneviewrs200834568
scholarrs200834568
googlers200834568
pharmgkbrs200834568
gwascentralrs200834568
openSNPrs200834568
23andMers200834568
23andMe allrs200834568
SNP Nexus

SNPshotrs200834568
SNPdbers200834568
MSV3drs200834568
GWAS Ctlgrs200834568
Max Magnitude0
ClinVar
Risk rs200834568(A;A)
Alt rs200834568(A;A)
Reference rs200834568(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene ZFPM2 ZFPM2-AS1
CLNDBN 46,XY sex reversal 9
Reversed 0
HGVS NC_000008.10:g.106810991G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144725.3,