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Variant (rsID / SNP)

rs807547

CLTCL1

rs807547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLTCL1. Location: chromosome 22, position 19,195,680. The table records no clinical significance for this variant.

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Reference-table entries

CLTCL1Not classified
Variant type
missense_variant
Chromosome / position
22:19195680
HGVS
NM_007098.4,c.3584A>G,p.Asn1195Ser
Allele change
Missense_N1195S

Public references

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