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rs766783183

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs766783183(A;G)
Make rs766783183(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position40750961
GeneKRT25
is asnp
is mentioned by
dbSNPrs766783183
ebirs766783183
HLIrs766783183
Exacrs766783183
Varsomers766783183
Maprs766783183
PheGenIrs766783183
hapmaprs766783183
1000 genomesrs766783183
hgdprs766783183
ensemblrs766783183
gopubmedrs766783183
geneviewrs766783183
scholarrs766783183
googlers766783183
pharmgkbrs766783183
gwascentralrs766783183
openSNPrs766783183
23andMers766783183
23andMe allrs766783183
SNP Nexus

SNPshotrs766783183
SNPdbers766783183
MSV3drs766783183
GWAS Ctlgrs766783183
Max Magnitude0
ClinVar
Risk rs766783183(G;G)
Alt rs766783183(G;G)
Reference rs766783183(A;A)
Significance Pathogenic
Disease Hypotrichosis 8 Autosomal recessive woolly hair 3
Variation info
Gene KRT25
CLNDBN Hypotrichosis 8 Autosomal recessive woolly hair 3
Reversed 0
HGVS NC_000017.10:g.38907213A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000201248.1, RCV000203575.1,