rs104893853

Orientation

plus

Stabilized

plus

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

Make rs104893853(A;A)

Make rs104893853(A;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4862854

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs104893853
dbSNP (classic)	rs104893853
ClinGen	rs104893853
ebi	rs104893853
HLI	rs104893853
Exac	rs104893853
Gnomad	rs104893853
Varsome	rs104893853
LitVar	rs104893853
Map	rs104893853
PheGenI	rs104893853
Biobank	rs104893853
1000 genomes	rs104893853
hgdp	rs104893853
ensembl	rs104893853
geneview	rs104893853
scholar	rs104893853
google	rs104893853
pharmgkb	rs104893853
gwascentral	rs104893853
openSNP	rs104893853
23andMe	rs104893853
SNPshot	rs104893853
SNPdbe	rs104893853
MSV3d	rs104893853
GWAS Ctlg	rs104893853

Max Magnitude

0

OMIM	142983
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893853(A;A) rs104893853(G;G)
Alt	rs104893853(A;A) rs104893853(G;G)
Reference	Rs104893853(C;C)
Significance	Pathogenic
Disease	Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Variation	info
Gene	MSX1
CLNDBN	Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Reversed	0
HGVS	NC_000004.11:g.4864581C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016011.25,