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rs786204684

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204684(C;T)
Make rs786204684(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35657955
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs786204684
ebirs786204684
HLIrs786204684
Exacrs786204684
Varsomers786204684
Maprs786204684
PheGenIrs786204684
hapmaprs786204684
1000 genomesrs786204684
hgdprs786204684
ensemblrs786204684
gopubmedrs786204684
geneviewrs786204684
scholarrs786204684
googlers786204684
pharmgkbrs786204684
gwascentralrs786204684
openSNPrs786204684
23andMers786204684
23andMe allrs786204684
SNP Nexus

SNPshotrs786204684
SNPdbers786204684
MSV3drs786204684
GWAS Ctlgrs786204684
Max Magnitude0
ClinVar
Risk rs786204684(T;T)
Alt rs786204684(T;T)
Reference rs786204684(C;C)
Significance Other
Disease Metaphyseal chondrodysplasia
Variation info
Gene CCDC107 RMRP
CLNDBN Metaphyseal chondrodysplasia, McKusick type
Reversed 1
HGVS NC_000009.11:g.35657952G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000169492.4,