rs121912985

Orientation

plus

Stabilized

plus

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

Make rs121912985(C;T)

Make rs121912985(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

87612186

Gene

DSPP

is a	snp
is	mentioned by
dbSNP	rs121912985
dbSNP (classic)	rs121912985
ClinGen	rs121912985
ebi	rs121912985
HLI	rs121912985
Exac	rs121912985
Gnomad	rs121912985
Varsome	rs121912985
LitVar	rs121912985
Map	rs121912985
PheGenI	rs121912985
Biobank	rs121912985
1000 genomes	rs121912985
hgdp	rs121912985
ensembl	rs121912985
geneview	rs121912985
scholar	rs121912985
google	rs121912985
pharmgkb	rs121912985
gwascentral	rs121912985
openSNP	rs121912985
23andMe	rs121912985
SNPshot	rs121912985
SNPdbe	rs121912985
MSV3d	rs121912985
GWAS Ctlg	rs121912985

Max Magnitude

0

OMIM	125485
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121912985(T;T)
Alt	rs121912985(T;T)
Reference	Rs121912985(C;C)
Significance	Pathogenic
Disease	Dentinogenesis imperfecta - Shield's type II
Variation	info
Gene	DSPP
CLNDBN	Dentinogenesis imperfecta - Shield's type II
Reversed	0
HGVS	NC_000004.11:g.88533338C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018347.27,