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Variant (rsID / SNP)

rs3748400

ZCCHC14

rs3748400 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZCCHC14. Location: chromosome 16, position 87,445,839. The table records no clinical significance for this variant.

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Reference-table entries

ZCCHC14Not classified
Variant type
missense_variant
Chromosome / position
16:87445839
HGVS
NM_015144.3,c.2488G>A,p.Val830Met
Allele change
Missense_V693M

Public references

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