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

rs606231233

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231233(G;T)
Make rs606231233(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position73362732
GeneKHDC3L
is asnp
is mentioned by
dbSNPrs606231233
ebirs606231233
HLIrs606231233
Exacrs606231233
Varsomers606231233
Maprs606231233
PheGenIrs606231233
hapmaprs606231233
1000 genomesrs606231233
hgdprs606231233
ensemblrs606231233
gopubmedrs606231233
geneviewrs606231233
scholarrs606231233
googlers606231233
pharmgkbrs606231233
gwascentralrs606231233
openSNPrs606231233
23andMers606231233
23andMe allrs606231233
SNP Nexus

SNPshotrs606231233
SNPdbers606231233
MSV3drs606231233
GWAS Ctlgrs606231233
Max Magnitude0
ClinVar
Risk rs606231233(T;T)
Alt rs606231233(T;T)
Reference rs606231233(G;G)
Significance Pathogenic
Disease Hydatidiform mole
Variation info
Gene KHDC3L
CLNDBN Hydatidiform mole, recurrent, 2
Reversed 0
HGVS NC_000006.11:g.74072455G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023914.3,