rs727502774

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs727502774(G;T)

Make rs727502774(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

35657756

Gene	CCDC107, RMRP

is a	snp
is	mentioned by
dbSNP	rs727502774
dbSNP (classic)	rs727502774
ClinGen	rs727502774
ebi	rs727502774
HLI	rs727502774
Exac	rs727502774
Gnomad	rs727502774
Varsome	rs727502774
LitVar	rs727502774
Map	rs727502774
PheGenI	rs727502774
Biobank	rs727502774
1000 genomes	rs727502774
hgdp	rs727502774
ensembl	rs727502774
geneview	rs727502774
scholar	rs727502774
google	rs727502774
pharmgkb	rs727502774
gwascentral	rs727502774
openSNP	rs727502774
23andMe	rs727502774
SNPshot	rs727502774
SNPdbe	rs727502774
MSV3d	rs727502774
GWAS Ctlg	rs727502774

Max Magnitude

0

ClinVar
Risk	rs727502774(A;A) rs727502774(T;T)
Alt	rs727502774(A;A) rs727502774(T;T)
Reference	Rs727502774(G;G)
Significance	Pathogenic
Disease	Metaphyseal chondrodysplasia
Variation	info
Gene	CCDC107 RMRP
CLNDBN	Metaphyseal chondrodysplasia, McKusick type
Reversed	1
HGVS	NC_000009.11:g.35657753C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015277.23,