rs398124254

Orientation

plus

Stabilized

plus

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

Make rs398124254(-;TGAAGC)

Make rs398124254(TGAAGC;TGAAGC)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

83908163

Gene

MLYCD

is a	snp
is	mentioned by
dbSNP	rs398124254
dbSNP (classic)	rs398124254
ClinGen	rs398124254
ebi	rs398124254
HLI	rs398124254
Exac	rs398124254
Gnomad	rs398124254
Varsome	rs398124254
LitVar	rs398124254
Map	rs398124254
PheGenI	rs398124254
Biobank	rs398124254
1000 genomes	rs398124254
hgdp	rs398124254
ensembl	rs398124254
geneview	rs398124254
scholar	rs398124254
google	rs398124254
pharmgkb	rs398124254
gwascentral	rs398124254
openSNP	rs398124254
23andMe	rs398124254
SNPshot	rs398124254
SNPdbe	rs398124254
MSV3d	rs398124254
GWAS Ctlg	rs398124254

Max Magnitude

0

ClinVar
Risk	rs398124254(TGAAGC;TGAAGC)
Alt	rs398124254(TGAAGC;TGAAGC)
Reference	Rs398124254(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MLYCD
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.83941768_83941769insTGAAGC
CLNSRC
CLNACC	RCV000081531.3,