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Variant (rsID / SNP)

rs61997220

ZC3H12D

rs61997220 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC3H12D. Location: chromosome 6, position 149,783,095. The table records no clinical significance for this variant.

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Reference-table entries

ZC3H12DNot classified
Variant type
missense_variant
Chromosome / position
6:149783095
HGVS
NM_207360.3,c.317A>G,p.Lys106Arg
Allele change
Missense_K106R

Public references

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