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rs121908602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908602(C;T)
Make rs121908602(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position105561395
GeneZFPM2
is asnp
is mentioned by
dbSNPrs121908602
ebirs121908602
HLIrs121908602
Exacrs121908602
Varsomers121908602
Maprs121908602
PheGenIrs121908602
hapmaprs121908602
1000 genomesrs121908602
hgdprs121908602
ensemblrs121908602
gopubmedrs121908602
geneviewrs121908602
scholarrs121908602
googlers121908602
pharmgkbrs121908602
gwascentralrs121908602
openSNPrs121908602
23andMers121908602
23andMe allrs121908602
SNP Nexus

SNPshotrs121908602
SNPdbers121908602
MSV3drs121908602
GWAS Ctlgrs121908602
Max Magnitude0
OMIM603693
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908602(T;T)
Alt rs121908602(T;T)
Reference rs121908602(C;C)
Significance Pathogenic
Disease Diaphragmatic hernia 3
Variation info
Gene ZFPM2
CLNDBN Diaphragmatic hernia 3
Reversed 0
HGVS NC_000008.10:g.106573623C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006503.2,