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Variant (rsID / SNP)

rs9910204

KRT37

rs9910204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT37. Location: chromosome 17, position 39,580,739. The table records no clinical significance for this variant.

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Reference-table entries

KRT37Not classified
Variant type
missense_variant
Chromosome / position
17:39580739
HGVS
NM_003770.5,c.37G>T,p.Gly13Cys
Allele change
Missense_G13C

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.