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Variant (rsID / SNP)

rs7578597

THADA

rs7578597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THADA. Location: chromosome 2, position 43,732,823. The table records no clinical significance for this variant.

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Reference-table entries

THADANot classified
Variant type
missense_variant
Chromosome / position
2:43732823
HGVS
NM_001083953.2,c.3559A>G,p.Thr1187Ala
Allele change
Missense_T1187A

Associated conditions / phenotypes

Diabetes Mellitus|Wolfram Syndrome 1|Type 2 Diabetes Mellitus|Lipid Metabolism Disorder

Public references

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