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Variant (rsID / SNP)

rs2567241

CLGN

rs2567241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLGN. Location: chromosome 4, position 141,323,162. The table records no clinical significance for this variant.

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Reference-table entries

CLGNNot classified
Variant type
missense_variant
Chromosome / position
4:141323162
HGVS
NM_001130675.2,c.478G>T,p.Ala160Ser
Allele change
Missense_A160S

Public references

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