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rs199952377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199952377(A;C)
Make rs199952377(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position19941796
GeneWDR35
is asnp
is mentioned by
dbSNPrs199952377
ebirs199952377
HLIrs199952377
Exacrs199952377
Varsomers199952377
Maprs199952377
PheGenIrs199952377
hapmaprs199952377
1000 genomesrs199952377
hgdprs199952377
ensemblrs199952377
gopubmedrs199952377
geneviewrs199952377
scholarrs199952377
googlers199952377
pharmgkbrs199952377
gwascentralrs199952377
openSNPrs199952377
23andMers199952377
23andMe allrs199952377
SNP Nexus

SNPshotrs199952377
SNPdbers199952377
MSV3drs199952377
GWAS Ctlgrs199952377
Max Magnitude0
ClinVar
Risk rs199952377(C;C)
Alt rs199952377(C;C)
Reference rs199952377(A;A)
Significance Pathogenic
Disease Cranioectodermal dysplasia 2
Variation info
Gene WDR35
CLNDBN Cranioectodermal dysplasia 2
Reversed 0
HGVS NC_000002.11:g.20141557A>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055830.1,