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rs751200138

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs751200138(C;T)
Make rs751200138(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position3067333
GeneMYOM1
is asnp
is mentioned by
dbSNPrs751200138
ebirs751200138
HLIrs751200138
Exacrs751200138
Varsomers751200138
Maprs751200138
PheGenIrs751200138
hapmaprs751200138
1000 genomesrs751200138
hgdprs751200138
ensemblrs751200138
gopubmedrs751200138
geneviewrs751200138
scholarrs751200138
googlers751200138
pharmgkbrs751200138
gwascentralrs751200138
openSNPrs751200138
23andMers751200138
23andMe allrs751200138
SNP Nexus

SNPshotrs751200138
SNPdbers751200138
MSV3drs751200138
GWAS Ctlgrs751200138
Max Magnitude0
ClinVar
Risk rs751200138(T;T)
Alt rs751200138(T;T)
Reference rs751200138(C;C)
Significance Probable-Pathogenic
Disease Non-immune hydrops fetalis
Variation info
Gene MYOM1
CLNDBN Non-immune hydrops fetalis
Reversed 0
HGVS NC_000018.9:g.3067331C>T
CLNSRC
CLNACC RCV000170579.1,