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rs754521978

From SNPedia

Orientationplus
Make rs754521978(-;-)
Make rs754521978(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position40395565
GenePRX
is asnp
is mentioned by
dbSNPrs754521978
ebirs754521978
HLIrs754521978
Exacrs754521978
Varsomers754521978
Maprs754521978
PheGenIrs754521978
hapmaprs754521978
1000 genomesrs754521978
hgdprs754521978
ensemblrs754521978
gopubmedrs754521978
geneviewrs754521978
scholarrs754521978
googlers754521978
pharmgkbrs754521978
gwascentralrs754521978
openSNPrs754521978
23andMers754521978
23andMe allrs754521978
SNP Nexus

SNPshotrs754521978
SNPdbers754521978
MSV3drs754521978
GWAS Ctlgrs754521978
Max Magnitude
ClinVar
Risk rs754521978(;)
Alt rs754521978(;)
Reference rs754521978(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene PRX
CLNDBN Charcot-Marie-Tooth disease, demyelinating, type 4f
Reversed 0
HGVS NC_000019.9:g.40901472delG
CLNSRC Quest Diagnostics
CLNACC RCV000201078.1,