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rs398124254

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124254(-;-)
Make rs398124254(-;TGAAGC)
Make rs398124254(TGAAGC;TGAAGC)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position83908163
GeneMLYCD
is asnp
is mentioned by
dbSNPrs398124254
ebirs398124254
HLIrs398124254
Exacrs398124254
Varsomers398124254
Maprs398124254
PheGenIrs398124254
hapmaprs398124254
1000 genomesrs398124254
hgdprs398124254
ensemblrs398124254
gopubmedrs398124254
geneviewrs398124254
scholarrs398124254
googlers398124254
pharmgkbrs398124254
gwascentralrs398124254
openSNPrs398124254
23andMers398124254
23andMe allrs398124254
SNP Nexus

SNPshotrs398124254
SNPdbers398124254
MSV3drs398124254
GWAS Ctlgrs398124254
Max Magnitude0
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,