Variant (rsID / SNP)

rs3887954

rs3887954 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRT3. Location: chromosome 12, position 53,186,088. The table records no clinical significance for this variant.

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Reference-table entries

KRT3Not classified

Variant type: missense_variant
Chromosome / position: 12:53186088
HGVS: NM_057088.3,c.1123C>G,p.Arg375Gly
Allele change: Missense_R375G

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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