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Variant (rsID / SNP)

rs6756597

ASB18

rs6756597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASB18. Location: chromosome 2, position 237,149,941. The table records no clinical significance for this variant.

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Reference-table entries

ASB18Not classified
Variant type
missense_variant
Chromosome / position
2:237149941
HGVS
NM_212556.4,c.310G>A,p.Ala104Thr
Allele change
Missense_A104T

Public references

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