|
No.
|
Position*
|
BC diplotype
|
AC diplotype
|
BB diplotype
|
AB diplotype
|
SNP novelty
|
SNP summary
|
|---|
|
1
|
7
|
C>A
|
C>A
|
C>A
|
C>A
|
Novel
|
Intron4:g.7 C>A
|
|
2
|
29
|
–
|
–
|
T>G
|
T>G
|
Novel
|
Intron4:29 T>G
|
|
3
|
36
|
–
|
–
|
A>C
|
A>C
|
Novel
|
Intron4:36 A>C
|
|
4
|
61
|
C>T
|
C>T
|
C>T
|
C>T
|
Novel
|
Intron4:61 C>T
|
|
5
|
71
|
C>G
|
C>G
|
C>G
|
C>G
|
Novel
|
Intron4:71 C>G
|
|
6
|
93
|
C>T
|
C>T
|
C>T
|
C>T
|
Novel
|
Intron4:93 C>T
|
|
7
|
119
|
–
|
C>A
|
–
|
C>A
|
Novel
|
Intron4:119 C>A
|
|
8
|
123
|
–
|
T>G
|
–
|
–
|
Novel
|
Intron4:123 T>G
|
|
9
|
129
|
C>T
|
C>T
|
C>T
|
C>T
|
Novel
|
Intron4:129 C>T
|
|
10
|
149
|
C>T
|
C>T
|
C>T
|
C>T
|
Novel
|
Intron4:149 C>T
|
- *The mentioned numbers refer to positions of the observed variants in PCR amplicons as well as in the submitted accession numbers (MG387135–MG387138) of the observed GHRL-based diplotypes. The observed variants were named following the nomenclature rules described in varnomen.hgvs.org/
