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rs797044636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044636(-;C)
Make rs797044636(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15516004
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs797044636
dbSNP (old)rs797044636
ClinGenrs797044636
ebirs797044636
HLIrs797044636
Exacrs797044636
Gnomadrs797044636
Varsomers797044636
Maprs797044636
PheGenIrs797044636
Biobankrs797044636
1000 genomesrs797044636
hgdprs797044636
ensemblrs797044636
gopubmedrs797044636
geneviewrs797044636
scholarrs797044636
googlers797044636
pharmgkbrs797044636
gwascentralrs797044636
openSNPrs797044636
23andMers797044636
23andMe allrs797044636
SNP Nexus

SNPshotrs797044636
SNPdbers797044636
MSV3drs797044636
GWAS Ctlgrs797044636
Max Magnitude0
ClinVar
Risk rs797044636(C;C)
Alt rs797044636(C;C)
Reference Rs797044636(-;-)
Significance Pathogenic
Disease Meckel syndrome type 6
Variation info
Gene CC2D2A
CLNDBN Meckel syndrome type 6
Reversed 0
HGVS NC_000004.11:g.15517627dupC
CLNSRC
CLNACC RCV000174035.1,