Variant (rsID / SNP)

rs7645550

rs7645550 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNMB3. Location: chromosome 3, position 178,968,634. The table records no clinical significance for this variant.

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Reference-table entries

KCNMB3Not classified

Variant type: missense_variant
Chromosome / position: 3:178968634
HGVS: NM_014407.3,c.157G>A,p.Ala53Thr
Allele change: Missense_A51T

Associated conditions / phenotypes

Type 2 Diabetes Mellitus

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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