rs895436485

Orientation

plus

Stabilized

plus

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

Make rs895436485(A;T)

Make rs895436485(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

94253674

Gene

SMARCAD1

is a	snp
is	mentioned by
dbSNP	rs895436485
dbSNP (classic)	rs895436485
ClinGen	rs895436485
ebi	rs895436485
HLI	rs895436485
Exac	rs895436485
Gnomad	rs895436485
Varsome	rs895436485
LitVar	rs895436485
Map	rs895436485
PheGenI	rs895436485
Biobank	rs895436485
1000 genomes	rs895436485
hgdp	rs895436485
ensembl	rs895436485
geneview	rs895436485
scholar	rs895436485
google	rs895436485
pharmgkb	rs895436485
gwascentral	rs895436485
openSNP	rs895436485
23andMe	rs895436485
SNPshot	rs895436485
SNPdbe	rs895436485
MSV3d	rs895436485
GWAS Ctlg	rs895436485

Max Magnitude

0

ClinVar
Risk	rs895436485(G;G) rs895436485(T;T)
Alt	rs895436485(G;G) rs895436485(T;T)
Reference	Rs895436485(A;A)
Significance	Pathogenic
Disease	Basan syndrome
Variation	info
Gene	SMARCAD1
CLNDBN	Basan syndrome
Reversed	0
HGVS	NC_000004.11:g.95174825A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000167536.6,