Have questions? Visit https://www.reddit.com/r/SNPedia

rs745776920

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745776920(C;T)
Make rs745776920(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position73363259
GeneKHDC3L
is asnp
is mentioned by
dbSNPrs745776920
ebirs745776920
HLIrs745776920
Exacrs745776920
Varsomers745776920
Maprs745776920
PheGenIrs745776920
hapmaprs745776920
1000 genomesrs745776920
hgdprs745776920
ensemblrs745776920
gopubmedrs745776920
geneviewrs745776920
scholarrs745776920
googlers745776920
pharmgkbrs745776920
gwascentralrs745776920
openSNPrs745776920
23andMers745776920
23andMe allrs745776920
SNP Nexus

SNPshotrs745776920
SNPdbers745776920
MSV3drs745776920
GWAS Ctlgrs745776920
Max Magnitude0
ClinVar
Risk rs745776920(T;T)
Alt rs745776920(T;T)
Reference rs745776920(C;C)
Significance Probable-Pathogenic
Disease Hydatidiform mole
Variation info
Gene KHDC3L
CLNDBN Hydatidiform mole, recurrent, 2
Reversed 0
HGVS NC_000006.11:g.74072982C>T
CLNSRC
CLNACC RCV000190600.1,